“Holistic Healing Home
for your animal companions"
Dr. Jeff
What follows is my own experience with homeopathic treatment of my Lyme disease. I have been asked several times to share this. Usually after a client's pet has received treatment. It is not meant for anyone else to emulate.


SINCE its original description nearly 25 years ago,1 Lyme disease has become recognized as an important infectious disease in the United States. The infection, which is caused by the tick- borne spirochete Borrelia burgdorferi, is now endemic in more than 15 states and has been responsible for focal outbreaks in some eastern coastal areas. Lyme borreliosis is also endemic in Europe and Asia, where certain aspects of the disease (erythema migrans, me- ningopolyneuritis, and acrodermatitis chronica atroph- icans) were described in the early and mid-20th cen- tury. These syndromes were linked conclusively in 1982 and 1983 with the recovery of a previously un- recognized spirochete from the tick vector and from infected patients.2,3


Since the last review of Lyme disease in the Journal 12 years ago,4 the number of scientific articles about this entity has increased substantially. During this pe- riod, the complete genome of the spirochete has been sequenced, animal models have been developed for studies of pathogenesis, guidelines for diagnosis and treatment have been established, and a vaccine has been developed to prevent the illness.



Since surveillance for Lyme disease was begun by the Centers for Disease Control in 1982, the number of reported cases has increased dramatically. Currently, about 15,000 cases are reported each year, making Lyme disease the most common vector-borne dis-ease in the United States.5 The disorder occurs primarily in three distinct foci: in the Northeast from Maine to Maryland, in the Midwest in Wisconsin and Minnesota, and in the West in northern California and Oregon. In Europe, Lyme borreliosis is widely established in forested areas. The highest reported frequencies of the disease are in middle Europe and Scandinavia, particularly in Germany, Austria, Slovenia, and Sweden.6 The infection is also found in Russia, China, and Japan.


Lyme borreliosis in all locations is transmitted by ticks of the Ixodes ricinus complex.7,8 These ticks have larval, nymphal, and adult stages; they require a blood meal at each stage. The risk of infection in a given area depends largely on the density of these ticks as well as their feeding habits and animal hosts, which have evolved differently in different locations. In the northeastern and north central United States, I. scapularis (also called I. dammini) ticks are abundant, and a highly efficient cycle of B. burgdorferi transmission occurs between immature larval and nymphal I. scapularis ticks and white-footed mice,8 resulting in high rates of infection in nymphal ticks and a high frequency of Lyme disease in humans during the late spring and summer months.5 The proliferation of deer, which are the preferred host of the adult tick, was a major factor in the emergence of epidemic Lyme disease in the northeastern United States during the late 20th century. In addition, I. scapularis is a vec- tor for the agents of human granulocytic ehrlichiosis and babesiosis. The vector ecology of B. burgdorferi is quite different in northern California and Oregon,9 where the frequency of Lyme disease is low.5 There, two intersecting cycles are necessary for the transmission of the disease. The spirochete is maintained in nature by the dusky-footed woodrat and I. neotomae ticks, which do not bite humans. Although nymphal I. paci- ficus ticks do bite humans, these ticks are usually not infected, because they prefer to feed on lizards, which are not susceptible to B. burgdorferi infection. Only the relatively few nymphal I. pacificus ticks that fed on infected woodrats when they were in the larval stage are responsible for the transmission of the spiro- chete to humans. Similarly, in the southeastern Unit- ed States, nymphal I. scapularis ticks feed primarily on lizards rather than rodents, and B. burgdorferi in- fection occurs rarely, if at all, in that part of the coun- try. There, a rash resembling erythema migrans but not caused by B. burgdorferi has been associated with the bite of the Lone Star tick.10 In Europe, the principal vector is I. ricinus, and in Asia, it is I. persulcatus.6 These ticks are also vectors of tick-borne encephalitis virus.



The structure of borrelia species, including B. burgdorferi, is similar to that of all spirochetes: a protoplasmic cylinder surrounded by periplasm con- taining the flagella, which is surrounded, in turn, by STEERE · 1

an outer membrane.11 The unique feature of borrelia species is that a number of their outer-membrane pro- teins are encoded by plasmid genes. The complete genome of B. burgdorferi (strain B31) has now been sequenced.12 The genome is quite small (approximate- ly 1.5 megabases) and consists of a highly unusual linear chromosome of 950 kilobases as well as 9 lin- ear and 12 circular plasmids. The remarkable aspect of the B. burgdorferi genome is its large number of sequences for predicted or known lipoproteins,12 including the plasmid-encod- ed outer-surface proteins (Osp) A through F. These and other differentially expressed outer-surface pro- teins presumably help the spirochete adapt to and survive in markedly different arthropod and mamma- lian environments.13 In addition, during early, dis- seminated infection, a surface-exposed lipoprotein, called VlsE, has been reported to undergo extensive antigenic variation.14 The organism has few proteins with biosynthetic activity and apparently depends on the host for most of its nutritional requirements.12 The genome contains no homologues for systems that specialize in the secretion of toxins or other virulence factors. The only known virulence factors of B. burg- dorferi are surface proteins that allow the spirochete to attach to mammalian cells. The causative agent of Lyme disease currently con- sists of three pathogenic species: B. burgdorferi, B. af- zelii, and B. garinii.15 Only B. burgdorferi strains have been found in the United States. In contrast, most of the illness in Europe is caused by B. afzelii and B. gari- nii, and only these two species have been found in Asia. The basic outlines of the disease are similar worldwide, but there are regional variations, primarily between the illness found in America and that found in Europe and Asia (Table 1).



The clinical manifestations of Lyme disease remain basically as they were presented in the Journal 12 years ago.4 However, much new information is avail- able about the pathogenesis of the disease, especially from animal models of the infection. Early infection consists of localized erythema migrans (stage 1), followed within days or weeks by disseminated infection that affects the nervous system, heart, or joints in particular (stage 2) and subsequently, within weeks or months, by late or persistent infection (stage 3). Skin Involvement and Early Disseminated Infection In at least 80 percent of patients in the United States, Lyme disease begins with a slowly expanding skin lesion, erythema migrans, which occurs at the site of the tick bite (Fig. 1).4 The skin lesion is frequently accompanied by influenza-like symptoms, such as ma- laise and fatigue, headache, arthralgias, myalgias, fe- ver, or regional lymphadenopathy, and these symp- VARIABLE Skin Acute phase Chronic phase Nervous system Acute phase Chronic phase Cardiac Acute phase Chronic phase Arthritis Acute phase Chronic phase Asymptomatic infection Antibody response NORTH AMERICA (BORRELIA BURGDORFERI) Erythema migrans faster spreading, more intensely in- flamed, and of briefer duration; frequent, possibly wide- spread hematogenous dissemination Acrodermatitis rarely reported Meningitis, severe headache, mild neck stiffness, less prominent radiculoneuritis Subtle sensory polyneuropathy without acrodermatitis Subtle encephalopathy, cognitive disturbance, slight intra- thecal antibody production Atrioventricular block and subtle myocarditis None reported More frequent oligoarticular arthritis, more intense joint inflammation Treatment-resistant arthritis in about 10 percent of pa- tients, probably due to autoimmune mechanism In about 10 percent of patients Expansion of response to many spirochetal proteins EUROPE AND ASIA (B. AFZELII OR B. GARINII) Erythema migrans slower spreading, less intensely inflamed, and of longer duration; less frequent hematogenous dis- semination, but possible regional or contiguous spread to other sites Acrodermatitis chronica atrophicans, caused primarily by B. afzelii Severe radicular pain and pleocytosis; less prominent head- ache and neck stiffness, caused particularly by B. garinii Subtle sensory polyneuropathy within areas affected by acro- dermatitis Severe encephalomyelitis, spasticity, cognitive abnormalities, and marked intrathecal antibody production, caused pri- marily by B. garinii Atrioventricular block and subtle myocarditis Dilated cardiomyopathy Less frequent oligoarticular arthritis, less intense joint in- flammation Persistent arthritis rare, probably not due to an autoimmune mechanism In more than 10 percent of patients Expansion of response to fewer spirochetal proteins 2 · STEERE The New England Journal of Medicine TABLE 1. COMPARISON OF LYME DISEASE IN NORTH AMERICA AND EUROPE AND ASIA.
toms may be the presenting manifestation of the illness. In Europe, erythema migrans is often an indo- lent, localized infection, whereas in the United States, this lesion is associated with more intense inflamma- tion and signs that often suggest dissemination of the spirochete.16 In one U.S. study, spirochetes were cultured from plasma samples in 50 percent of pa- tients with erythema migrans.17 A number of mechanisms may aid in the dissemi- nation of B. burgdorferi. For example, the sequences of OspC vary considerably among strains, and only a few of the groups of sequences are associated with disseminated disease.18 Spreading through skin and other tissue matrixes may be facilitated by the binding of human plasminogen and its activators to the sur- face of the spirochete.19 During the dissemination and homing to specific sites, the organism attaches to cer- tain host integrins,20,21 matrix glycosaminoglycans,22 and extracellular-matrix proteins.23 For example, bor- relia decorin-binding proteins A and B bind decorin, a glycosaminoglycan on collagen fibrils, which may explain why the organism is commonly aligned with collagen fibrils in the extracellular matrix in the heart, nervous system, or joints.22 In a recent report, decorin-deficient mice had more limited spirochetal colonization of joints and milder arthritis than nor- mal mice of the same strain that expressed decorin.24 As shown definitively in mice, inflammatory in- nate immune responses are critical in the control of early, disseminated infection.25,26 Spirochetal lipopro- teins, which bind the CD14 molecule and toll-like receptor 2 on macrophages, are potent activators of the innate immune response, leading to the produc- tion of macrophage-derived inflammatory cytokines.27 In addition, type 1 helper T (Th1) cells, which are part of the adaptive immune response, are prominent early in the infection in mice.28 In humans, infiltrates of macrophages and T cells in erythema migrans le- sions express messenger RNA for both inflammatory and antiinflammatory cytokines.29 Particularly in dis- seminated infection, adaptive T-cell and B-cell re- sponses in lymph nodes lead to the production of an- tibody against many components of the organism.30,31 Despite the innate and adaptive immune respons- es, B. burgdorferi may sometimes survive in certain sites. In European patients, especially elderly women with B. afzelii infection, a chronic, slowly progressive skin condition called acrodermatitis chronica atroph- icans may develop on sun-exposed acral surfaces. The organism has been cultured from such lesions as long as 10 years after the onset of the disease.32 In one study, the infiltrates of T cells and macrophages in these lesions had a restricted cytokine profile, with lit- tle or no production of interferon-g,29 which may ex- plain in part why the immune response is ineffective in eradicating the spirochete. Consistent with this hy- pothesis, ultraviolet B irradiation of C3H mice infect- ed with B. burgdorferi decreased the Th1 response.33 Neurologic Involvement Within weeks, during or shortly after the period of early, disseminated infection, objective signs and symptoms of acute neuroborreliosis develop in about 15 percent of untreated patients in the United States.4 Possible manifestations include lymphocytic menin- gitis with episodic headache and mild neck stiffness, subtle encephalitis with difficulty with mentation, cra- nial neuropathy (particularly unilateral or bilateral fa- cial palsy), motor or sensory radiculoneuritis, mono- neuritis multiplex, cerebellar ataxia, or myelitis.34,35 In children, the optic nerve may also be affected be- cause of inflammation or increased intracranial pres- sure, which may lead to blindness.36 Even in untreat- ed patients, acute neurologic abnormalities typically improve or resolve within weeks or months. The spread of B. burgdorferi within the nervous sys- tem has been demonstrated in nonhuman primates,37 the only known animal model of neuroborreliosis. In immunosuppressed monkeys, which had a larger spi- rochetal burden than did immunocompetent animals, B. burgdorferi infiltrated the leptomeninges, motor and sensory nerve roots, and dorsal-root ganglia, but not the brain parenchyma.38 In the peripheral nerv- ous system, spirochetes were seen in the perineurium, the connective-tissue sheath surrounding each bun- dle of peripheral-nerve fibers. In up to 5 percent of untreated patients, B. burg- dorferi may cause chronic neuroborreliosis, sometimes after long periods of latent infection.39 In both the United States and Europe, a chronic axonal polyneu- ropathy may develop, manifested primarily as spinal radicular pain or distal paresthesias.35,40 Electromyo- grams typically show diffuse involvement of both proximal and distal nerve segments. In Europe, B. gar- inii may cause chronic encephalomyelitis, character- ized by spastic paraparesis, cranial neuropathy, or cog- nitive impairment with marked intrathecal production of antibodies against the spirochete.35 In the United States, a mild, late neurologic syndrome has been re- ported, called Lyme encephalopathy, manifested pri- marily by subtle cognitive disturbances.39,41 Although there are no inflammatory changes in the cerebro- spinal fluid, the intrathecal production of antibodies against the spirochete can often be demonstrated. Nei- ther single-photon-emission computed tomography of the brain nor neuropsychological tests of memory have sufficient specificity to be helpful in the diag- nosis. Lyme encephalopathy may be treated successful- ly with a one-month course of intravenous ceftriaxone therapy,42 but immune-mediated or postinfectious phenomena may also play a part in the pathogenesis of these syndromes. One unusual case of B. burgdor- feri–induced meningoencephalitis and cerebral vas- culitis has been reported that was unresponsive to an- tibiotics.43 In this case, a T-cell clone recovered from the cerebrospinal fluid responded both to spirochet- al epitopes and to autoantigens. STEERE · 3
The New England Journal of Medicine Cardiac Involvement Within several weeks after the onset of disease, about 5 percent of untreated patients have acute cardi- ac involvement — most commonly fluctuating degrees of atrioventricular block, occasionally acute myoperi- carditis or mild left ventricular dysfunction, and rare- ly cardiomegaly or fatal pancarditis.4 In C3H mice, cardiac infiltrates of macrophages and T cells secrete inflammatory cytokines.44 In these mice, the killing of spirochetes through cellular immune mechanisms seems to be the dominant factor in the resolution of the cardiac lesion. In mice with severe combined im- munodeficiency, immune serum resolves arthritis but not carditis.45 In Europe, B. burgdorferi has been iso- lated from endomyocardial-biopsy samples from sev- eral patients with chronic dilated cardiomyopathy.46,47 However, this complication has not been observed in the United States.48 Joint Involvement Months after the onset of illness, about 60 per- cent of untreated patients in the United States begin to have intermittent attacks of joint swelling and pain, primarily in large joints, especially the knee.4 Synovial tissue from affected patients shows synovial hyper- trophy, vascular proliferation, and a marked infiltration of mononuclear cells, sometimes with pseudolymph- oid follicles that are reminiscent of a peripheral lymph node.49 During attacks of arthritis, innate immune responses to B. burgdorferi lipoproteins are found, and g/d T cells in joint fluid may aid in this re- sponse.50 In addition, there are marked adaptive im- mune responses to many spirochetal proteins.31,51 A borrelia-specific, inflammatory Th1 response is con- centrated in joint fluid,52,53 but antiinflammatory (Th2) cytokines are also present.53 Furthermore, pa- tients with Lyme arthritis usually have higher bor- relia-specific antibody titers than patients with any other manifestation of the illness, including late neu- roborreliosis.31,54 B A Figure 1. The Nymphal Ixodes scapularis Tick (Panel A) and Various Erythema Migrans Lesions (Panels B, C, and D). Lyme disease usually begins with a slowly expanding skin lesion, erythema migrans, which occurs at the site of a tick bite. Panel A shows a tiny (1 to 2 mm in diameter), nymphal I. scapularis tick (arrow) attached near the neck of a child. Panel B shows a classic erythema migrans lesion (9 cm in diameter) near the axilla. The lesion has partial central clearing, a bright red outer border, and a target center. Panel C shows a pale, homogeneous erythema migrans lesion (12 cm in diameter) on the back of a knee. Panel D shows an erythema migrans lesion (10 cm in diameter) with a vesicular center on the back of a knee. In each instance, Borrelia burgdorferi was isolated from a skin-biopsy sample of the lesion. (Photographs provided courtesy of Dr. Vijay Sikand, East Lyme, Conn., and the SmithKline Beecham Lyme Disease Vaccine Trial.) 4 · STEERE
C D The infection of inbred strains of mice has shown the importance of genetic factors in determining the severity of arthritis.25 Severe, acute arthritis develops in C3H/HeJ mice that are infected with B. burgdorferi55; antibody against a 37-kd arthritis-resolving protein is critical in the resolution of the arthritis.56 In con- trast, arthritis does not develop in B. burgdorferi– infected C57BL/6 mice.55 The components of the immune response that account for these differences between strains are not yet clear, but effective innate immune responses seem to be important in resist- ance to arthritis.25,26 After several brief attacks of arthritis, some patients may have persistent joint inflammation. In about 10 percent of patients, particularly those with HLA- DRB1*0401 or related alleles,57 the arthritis persists in the knees for months or even several years after 30 days of intravenous antibiotic therapy or 60 days of oral antibiotic therapy.58 In my experience, poly- merase-chain-reaction (PCR) tests for B. burgdorferi DNA in synovium or joint fluid are almost always neg- ative after this treatment,59,60 suggesting that the live spirochetes have been eradicated. Treatment-resistant arthritis and treatment-responsive arthritis differ pri- marily in the cellular and humoral immune responses to OspA.51,61 Such responses may be perpetuated after antibiotic treatment by OspA antigens that have been retained in the patients’ dendritic cells. However, OspA antigens are not detectable in the synovial tissue of such patients by immunoperoxidase techniques.60 Autoimmunity may develop within the inflamma- tory milieu of affected joints in these patients be- STEERE · 5
cause of molecular mimicry between an immuno- dominant T-cell epitope of OspA (OspA165–173) of B. burgdorferi and human-lymphocyte-function–asso- ciated antigen 1 (hLFA-1aL332–340),62 an adhesion mol- ecule that is highly expressed on T cells in synovium. T cells that react to OspA165–173 are concentrated in the joints of these patients.63 When hLFA-1a is L332–340 processed and presented by the HLA-DRB1*0401 molecule, this self peptide may behave as a partial agonist for such cells.64 However, it may not be the only relevant autoantigen in treatment-resistant Lyme arthritis.



The culture of B. burgdorferi from specimens in Barbour–Stoenner–Kelly medium permits a defini- tive diagnosis. However, except in the case of a few patients with acrodermatitis, positive cultures have been obtained only early in the illness, primarily from biopsy samples of erythema migrans lesions,65 less often from plasma samples,17 and only occasion- ally from cerebrospinal fluid samples in patients with meningitis.34 Later in the infection, PCR testing is greatly superior to culture in the detection of B. burgdorferi in joint fluid.59 B. burgdorferi has not been isolated from the cerebrospinal fluid of patients with chronic neuroborreliosis, and B. burgdorferi DNA has been detected in cerebrospinal fluid sam- ples in only a small number of such patients.66 The Lyme urine antigen test, which has given grossly un- reliable results,67 should not be used to support the diagnosis of Lyme disease. In patients in the United States, the diagnosis is usu- ally based on the recognition of the characteristic clin- ical findings, a history of exposure in an area where the disease is endemic, and except in patients with erythe- ma migrans, an antibody response to B. burgdorferi by enzyme-linked immunosorbent assay (ELISA) and Western blotting, interpreted according to the criteria of the Centers for Disease Control and Prevention and the Association of State and Territorial Public Health Laboratory Directors (Table 2).68,69 In Eu- rope, where there is less expansion of the antibody response, no single set of criteria for the interpreta- tion of immunoblots results in high levels of sensi- tivity and specificity in all countries.70 Serodiagnostic tests are insensitive during the first several weeks of infection. In the United States, ap- proximately 20 to 30 percent of patients have posi- tive responses, usually of the IgM isotype, during this period,54,71 but by convalescence two to four weeks later, about 70 to 80 percent have seroreactivity, even after antibiotic treatment. After one month, the ma- jority of patients with active infection have IgG an- tibody responses.54 In persons who have been ill for longer than one month, a positive IgM test alone is likely to represent a false positive result; therefore, such a response should not be used to support the di-


TABLE 2. CASE DEFINITION OF LYME DISEASE FOR NATIONAL SURVEILLANCE.* Erythema migrans, observed by a physician. This skin lesion expands slowly over a period of days or weeks to form a large, round lesion, often with central clearing. To be counted for surveillance purposes, a solitary le- sion must reach a size of at least 5 cm. At least one subsequent manifestation and laboratory evidence of infection Nervous system: Lymphocytic meningitis, cranial neuritis, radiculoneu- ropathy, or rarely, encephalomyelitis, alone or in combination. For en- cephalomyelitis to be counted for surveillance purposes, there must be evidence in cerebrospinal fluid of the intrathecal production of anti- body against Borrelia burgdorferi. Cardiovascular system: Acute-onset, high-grade (2nd- or 3rd-degree) atrioventricular conduction defects that resolve in days or weeks and are sometimes associated with myocarditis. Musculoskeletal system: Recurrent, brief attacks (lasting weeks to months) of objectively confirmed joint swelling in one or a few joints, sometimes followed by chronic arthritis in one or a few joints. Laboratory evidence: Isolation of B. burgdorferi from tissue or body fluid or detection of diagnostic levels of antibody against the spirochete by the two-test approach of enzyme-linked immunosorbent assay and Western blotting, interpreted according to the criteria of the Centers for Disease Control and Prevention and the Association of State and Territorial Public Health Laboratory Directors.† *Adapted from recommendations made by the Centers for Disease Con- trol and Prevention.68,69 †In a person with acute disease of less than one month’s duration, IgM and IgG antibody responses should be measured in serum samples ob- tained during the acute and convalescent phases. A Western blot for IgM antibodies is considered positive if at least two of the following three bands are present: 23, 39, and 41 kd. A blot for IgG antibodies is considered pos- itive if at least 5 of the following 10 bands are present: 18, 23, 28, 30, 39, 41, 45, 58, 66, and 93 kd. Only the IgG response should be used to sup- port the diagnosis after the first month of infection; after that time, an IgM response alone is likely to represent a false positive result. agnosis after the first month of infection. In patients with acute neuroborreliosis, especially those with meningitis, the intrathecal production of IgM, IgG, or IgA antibody against B. burgdorferi may often be demonstrated by antibody-capture enzyme immu- noassay,72 but this test is less often positive in those with chronic neuroborreliosis. After antibiotic treatment, antibody titers fall slow- ly, but IgG and even IgM responses may persist for many years after treatment.73 Thus, even an IgM re- sponse cannot be interpreted as a demonstration of re- cent infection or reinfection unless the appropriate clinical characteristics are present. In addition, B. burg- dorferi may cause asymptomatic infection. In a trial of Lyme disease vaccine in the United States in which subjects were followed prospectively for 20 months, IgG seroconversion was demonstrated on Western blotting in about 10 percent of subjects who had no symptoms of the infection.74 In a study of seroprev- alence in Sweden, more than half the subjects who were seropositive by ELISA did not remember hav- ing symptoms of Lyme borreliosis.75 In tests that use whole, sonicated spirochetes as the antigen prepara- tion, vaccination for Lyme disease may cause positive IgG results by ELISA, but vaccine-induced antibody responses can usually be differentiated from infec- 6 · STEERE The New England Journal of Medicine
tion-induced responses by Western blotting.74 If pa- tients with past or asymptomatic infection or vaccine- induced immunity have symptoms caused by another illness, there is a danger that the symptoms will be attributed incorrectly to Lyme disease. Several second- generation tests that use recombinant spirochetal proteins or synthetic peptides have shown promising results.76,77 TREATMENT AND OUTCOME Evidence-based treatment recommendations for Lyme disease, similar to those reported in the Journal 12 years ago,4 were recently presented by the Infec- tious Diseases Society of America.78 The American College of Physicians has also developed an algorithm to guide testing and treatment according to the prob- ability of Lyme disease before testing.79 For early lo- calized or disseminated infection, treatment with dox- ycycline for 14 to 21 days is recommended in persons older than eight years of age, except for pregnant women (Table 3). An advantage of doxycycline is its ef- ficacy against the agent of human granulocytic ehrlich- iosis, a possible coinfecting agent. Amoxicillin, the second-choice alternative, should be used in children and pregnant women. In patients who are allergic to either of these drugs, cefuroxime axetil is a third- choice alternative. Erythromycin or its congeners, which are fourth-choice alternatives, are recommended only for patients who are unable to take doxycycline, amoxicillin, or cefuroxime axetil. Because maternal– fetaltransmissionof B.burgdorferiseemstooccurrare- ly, if at all,81 standard therapy for the manifestation of the illness is recommended for pregnant women; dox- ycycline should be avoided in pregnant women. In multicenter studies of patients with erythema mi- grans, similar results were obtained with doxycycline, amoxicillin, and cefuroxime axetil, and more than 90 percent of patients had satisfactory outcomes.82,83 Al- though some patients had subjective symptoms after treatment, objective evidence of persistent infection or relapse was rare, and retreatment was usually not needed. Intravenous ceftriaxone, although effective, was not superior to oral agents as long as the patient did not have objective evidence of neurologic involve- ment.84 In contrast to second- and third-generation cephalosporin antibiotics, first-generation cephalo- sporins, such as cephalexin, were ineffective.85 For patients with objective evidence of neurologic abnormalities, a two-to-four-week course of intrave- nous ceftriaxone is most commonly given.39,42,86 Par- enteral therapy with cefotaxime or penicillin G may be a satisfactory alternative.87 The signs and symptoms of acute neuroborreliosis usually resolve within weeks, but those of chronic neuroborreliosis improve slowly over a period of months. Objective evidence of relapse is rare after a four-week course of therapy. In Europe, oral doxycycline may be adequate therapy for acute neuroborreliosis.88 Although this medication may be used successfully in the United States in patients with facial palsy alone, it is important to assess whether such patients have more diffuse involvement of the nervous system, which is best treated with intravenous therapy. In my experience, doxycycline is not effective for the treatment of chronic neuroborreliosis. In pa- tients with atrioventricular nodal block with a PR in- terval greater than 0.3 second, therapy with one of the intravenous regimens for at least part of the course and cardiac monitoring are recommended, but the insertion of a permanent pacemaker is not necessary. Either the oral or intravenous regimens, most often oral doxycycline or intravenous ceftriaxone, are usu- ally effective for the treatment of Lyme arthritis.58,86 Oral therapy is easier to administer, is associated with fewer side effects, and is considerably less expensive.89 Its disadvantage is that some patients treated with oral agents have subsequently had overt neuroborre- liosis, which may require intravenous therapy for suc- cessful treatment.58 Despite treatment with either oral or intravenous antibiotic therapy, about 10 per- cent of patients in the United States have persistent joint inflammation for months or even several years af- ter two months or more of oral antibiotic therapy or one month or more of intravenous antibiotic thera- py.58 If patients have persistent arthritis despite this treatment and if the results of PCR testing of joint fluid are negative, they may be treated with antiin- flammatory agents or arthroscopic synovectomy. After appropriately treated Lyme disease, a small percentage of patients continue to have subjective symptoms — primarily musculoskeletal pain, neu- rocognitive difficulties, or fatigue — that may last for years. This disabling syndrome, which is sometimes called “chronic Lyme disease” or “post–Lyme disease syndrome,” is similar to chronic fatigue syndrome or fibromyalgia.90 This postinfectious syndrome occurs more frequently in patients whose symptoms are sug- gestive of early dissemination of the spirochete to the nervous system, particularly if treatment is de- layed.91,92 However, in a large study, the frequency of symptoms of pain and fatigue was no greater in pa- tients who had had Lyme disease than in age-matched subjects who had not had this infection.93 In a study of patients with post–Lyme disease syndrome who received either intravenous ceftriax- one for 30 days followed by oral doxycycline for 60 days or intravenous and oral placebo preparations for the same duration, there were no significant dif- ferences between the groups in the percentage of pa- tients who said that their symptoms had improved, gotten worse, or stayed the same.94 Such patients are best treated symptomatically rather than with pro- longed courses of antibiotic therapy. Prolonged cef- triaxone therapy for unsubstantiated Lyme disease has resulted in biliary complications95; and in one re- ported case, the prolonged administration of cefo- taxime resulted in death.96 STEERE · 7
The New England Journal of Medicine TABLE 3. TREATMENT AND VACCINATION REGIMENS FOR LYME DISEASE.* VARIABLE Early infection (local or disseminated) Adults In case of doxycycline or amoxicillin allergy Children In case of penicillin allergy Neurologic abnormalities (early or late) Adults In case of ceftriaxone or penicillin allergy Facial palsy alone Children Arthritis (intermittent or chronic) Cardiac abnormalities First-degree atrioventricular block High-degree atrioventricular block (PR interval >0.3 sec) Pregnant women Vaccination REGIMEN Doxycycline, 100 mg orally twice daily for 14 to 21 days Amoxicillin, 500 mg orally three times daily for 14 to 21 days Cefuroxime axetil, 500 mg orally twice daily for 14 to 21 days Erythromycin, 250 mg orally 4 times a day for 14 to 21 days Amoxicillin, 250 mg orally 3 times a day or 50 mg per kilogram of body weight per day in 3 divided doses for 14 to 21 days Cefuroxime axetil, 125 mg orally twice daily or 30 mg per kg per day in 2 divided doses for 14 to 21 days Erythromycin, 250 mg orally 3 times a day or 30 mg per kg per day in 3 divided doses for 14 to 21 days Ceftriaxone, 2 g IV once a day for 14 to 28 days Cefotaxime, 2 g IV every 8 hr for 14 to 28 days Penicillin G sodium, 3.3 million U IV every 4 hr (20 million U per day) for 14 to 28 days Doxycycline, 100 mg orally 3 times a day for 30 days† Oral regimens may be adequate Ceftriaxone, 75 to 100 mg per kg per day (maximum, 2 g) IV once a day for 14 to 28 days Cefotaxime, 150 mg per kg per day in 3 or 4 divided doses (max- imum, 6 g) for 14 to 28 days Penicillin G sodium, 200,000 to 400,000 U per kg per day in 6 divided doses for 14 to 28 days Oral regimens listed above for 30 to 60 days or IV regimens listed above for 14 to 28 days Oral regimens listed above for 14 to 21 days IV regimens listed above and cardiac monitoring‡ Standard therapy for manifestation of the illness; avoid doxycycline L-OspA in adjuvant, 30 μg intramuscularly, at 0, 1, and 12 months (or 0, 1, and 2 months)§ *The recommendations for antibiotics are based on the guidelines of the Infectious Diseases Society of America.78 The recommendations regarding vaccine are based on the results of a phase 3 efficacy and safety trial74 and on the recom- mendations of the Advisory Committee on Immunization Practices of the Centers for Disease Control and Prevention.80 IV denotes intravenously. †This regimen may be ineffective for late neuroborreliosis. ‡Once the patient’s condition has stabilized, the course may be completed with oral therapy. §The third dose should be given in April. Booster injections may be necessary every one to three years to maintain protection. L-OspA is full-length OspA to which the lipid moiety has been added after translation. Should I. scapularis tick bites be treated with an- tibiotic prophylaxis? In studies, the frequency of Lyme disease after a recognized tick bite has been only about 1 percent,97 perhaps because the tick must usu- ally be attached for at least 24 hours for transmission to occur.98 Thus, if an attached tick is removed quickly, no other treatment is usually necessary. However, a single 200-mg dose of doxycycline effectively pre- vents Lyme disease when given within 72 hours after the tick bite occurs.99 PREVENTION Protective measures for the prevention of Lyme disease may include the avoidance of tick-infested ar- eas, the use of protective clothing, the use of repel- lents and acaricides, tick checks, and modifications of landscapes in or near residential areas.80 In addition, a vaccine for Lyme disease, consisting of recombi- nant OspA in adjuvant, is now commercially available in the United States (Table 3). In a phase 3 efficacy and safety trial, the efficacy of the vaccine in the pre- vention of definite Lyme disease was 49 percent after two injections and 76 percent after three injections.74 The most important factor in protection was the strength of the antibody response to the protective epitope of OspA. Injection of the vaccine was asso- ciated with mild-to-moderate local or systemic reac- tions lasting a median of three days. Although T-cell responses to OspA have been associated with treat- ment-resistant Lyme arthritis,51,62 recipients of vac- cine and placebo did not differ significantly in the development of arthritis or any other late syndrome after vaccination. Thus, vaccination seems not to du- plicate the conditions necessary for the induction of autoimmunity in joints that can occur in the natural infection. 8 · STEERE
The Advisory Committee on Immunization Prac- tices of the Centers for Disease Control and Preven- tion advises that vaccination for Lyme disease should be considered by persons 15 to 70 years old who live in or visit high-risk areas and have frequent or pro- longed exposure to I. scapularis ticks.80 Vaccination is not recommended for persons with minimal or no exposure to such ticks. Patients who are treated for erythema migrans may become reinfected and are candidates for vaccination. However, patients with Lyme arthritis usually have high antibody titers to many spirochetal proteins and seem not to become reinfected. Therefore, vaccination is probably not nec- essary in these patients. To achieve a protective re- sponse, it is recommended that persons receive three injections, the second vaccination 1 month after the first and the third 12 months after the first, although equivalent antibody titers can be obtained by giving the third injection at 2 months.100 The third injection should be given in April so that the patient will have sufficient antibody titers against OspA during the summer. Since antibody titers wane rather quickly,74 booster injections may need to be given every one to three years to maintain protection, but official recommen- dations have not yet been made regarding this issue. Because the vaccine was tested in healthy subjects, little information is available regarding the safety of vaccination in persons with other diseases, such as rheumatoid arthritis. The vaccine has not yet been approved for use in children. It is a personal decision whether to take a preven- tive approach to Lyme disease that involves vaccina- tion and repeated booster injections or to take a re- active approach that requires antibiotic treatment only if symptoms of tick-borne infection develop. Either way, vigilance for tick bites must continue, since the vaccine is not always effective against Lyme disease and does not protect against other possible tick-borne infections. Supported by a grant (AR-20358) from the National Institutes of Health, by a cooperative agreement (CCU110291) with the Centers for Disease Control and Prevention, and by grants from the Mathers Foundation, the Lyme/Arthritis Research Foundation, and the Eshe Fund. I am indebted to Drs. Jennifer Coburn, David Dennis, Lisa Glickstein, Barbara Johnson, Janis Weis, and Nord Zeidler for their review of the manuscript; and to Ms. Colleen Fitzpatrick for help with preparation of the manuscript. REFERENCES 1. Steere AC, Malawista SE, Snydman DR, et al. Lyme arthritis: an epi- demic of oligoarticular arthritis in children and adults in three Connecticut communities. Arthritis Rheum 1977;20:7-17. 2. Burgdorfer W, Barbour AG, Hayes SF, Benach JL, Grunwaldt E, Davis JP. Lyme disease — a tick-borne spirochetosis? Science 1982;216:1317-9. 3. Steere AC, Grodzicki RL, Kornblatt AN, et al. The spirochetal etiology of Lyme disease. N Engl J Med 1983;308:733-40. 4. Steere AC. Lyme disease. N Engl J Med 1989;321:586-96. 5. Orloski KA, Hayes EB, Campbell GL, Dennis DT. Surveillance for Lyme disease — United States, 1992–1998. MMWR CDC Surveill Summ 2000;49(SS-3):1-11. 6. Stanek G, Satz N, Strle F, Wilske B. Epidemiology of Lyme borreliosis. In: Weber K, Burgdorfer W, eds. Aspects of Lyme borreliosis. Berlin, Ger- many: Springer-Verlag, 1993:358-70. 7. Lane RS, Piesman J, Burgdorfer W. Lyme borreliosis: relation of its causative agent to its vectors and hosts in North America and Europe. Annu Rev Entomol 1991;36:587-609. 8. Spielman A. The emergence of Lyme disease and human babesiosis in a changing environment. Ann N Y Acad Sci 1994;740:146-56. 9. Brown RN, Lane RS. Lyme disease in California: a novel enzootic transmission cycle of Borrelia burgdorferi. Science 1992;256:1439-42. 10. Campbell GL, Paul WS, Schriefer ME, Craven RB, Robbins KE, Den- nis DT. Epidemiologic and diagnostic studies of patients with suspected early Lyme disease, Missouri, 1990–1993. J Infect Dis 1995;172:470-80. 11. Barbour AG, Hayes SF. Biology of Borrelia species. Microbiol Rev 1986;50:381-400. 12. Fraser CM, Casjens S, Huang WM, et al. Genomic sequence of a Lyme disease spirochete, Borrelia burgdorferi. Nature 1997;390:580-6. 13. de Silva AM, Fikrig E. Arthropod- and host-specific gene expression by Borrelia burgdorferi. J Clin Invest 1997;99:377-9. 14. Zhang J-R, Norris SJ. Genetic variation of the Borrelia burgdorferi gene vlsE involves cassette-specific, segmental gene conversion. Infect Im- mun 1998;66:3698-704. 15. Baranton G, Postic D, Saint Girons I, et al. Delineation of Borrelia burgdorferi sensu stricto, Borrelia garinii sp. nov., and group VS461 asso- ciated with Lyme borreliosis. Int J Syst Bacteriol 1992;42:378-83. 16. Strle F, Nadelman RB, Cimperman J, et al. Comparison of culture- confirmed erythema migrans caused by Borrelia burgdorferi sensu stricto in New York State and by Borrelia afzelii in Slovenia. Ann Intern Med 1999;130:32-6. 17. Wormser GP, Bittker S, Cooper D, Nowakowski J, Nadelman RB, Pa- via C. Comparison of the yields of blood cultures using serum or plasma from patients with early Lyme disease. J Clin Microbiol 2000;38:1648-50. 18. Seinost G, Dykhuizen DE, Dattwyler RJ, et al. Four clones of Borrelia burgdorferi sensu stricto cause invasive infection in humans. Infect Immun 1999;67:3518-24. 19. Coleman JL, Gebbia JA, Piesman J, Degen JL, Bugge TH, Benach JL. Plasminogen is required for efficient dissemination of B. burgdorferi in ticks and for enhancement of spirochetemia in mice. Cell 1997;89:1111-9. 20. Coburn J, Leong JM, Erban JK. Integrin aIIbb3 mediates binding of the Lyme disease agent Borrelia burgdorferi to human platelets. Proc Natl Acad Sci U S A 1993;90:7059-63. 21. Coburn J, Magoun L, Bodary SC, Leong KM. Integrins av b3 and a5b1 mediate attachment of Lyme disease spirochetes to human cells. Infect Im- mun 1998;66:1946-52. 22. Guo BP, Brown EL, Dorward DW, Rosenberg LC, Hook M. Decorin- binding adhesins from Borrelia burgdorferi. Mol Microbiol 1998;30:711- 23. 23. Probert WS, Johnson BJB. Identification of a 47 kDa fibronectin- binding protein expressed by Borrelia burgdorferi isolate B31. Mol Micro- biol 1998;30:1003-15. 24. Brown EL, Wooten RM, Johnson BJB, et al. Resistance to Lyme dis- ease in decorin-deficient mice. J Clin Invest 2001;107:845-52. 25. Weiss JJ, McCracken BA, Ma Y, et al. Identification of quantitative trait loci governing arthritis severity and humoral responses in the murine model of Lyme disease. J Immun 1999;162:948-56. 26. Barthold SW, de Souza M. Exacerbation of Lyme arthritis in beige mice. J Infect Dis 1995;172:778-84. 27. Hirschfeld M, Kirschning CJ, Schwander R, et al. Inflammatory sig- naling by Borrelia burgdorferi lipoproteins is mediated by toll-like receptor 2. J Immunol 1999;163:2382-6. 28. Kang I, Barthold SW, Persing DH, Bockenstedt LK. T-helper-cell cy- tokines in the early evolution of murine Lyme arthritis. Infect Immun 1997;65:3107-11. 29. Muellegger RR, McHugh G, Ruthazer R, Binder B, Kerl H, Steere AC. Differential expression of cytokine mRNA in skin specimens from pa- tients with erythema migrans or acrodermatitis chronica atrophicans. J In- vest Dermatol 2000;115:1115-23. 30. Krause A, Brade V, Schoerner C, Solbach W, Kalden JR, Burmester GR. T cell proliferation induced by Borrelia burgdorferi in patients with Lyme borreliosis: autologous serum required for optimum stimulation. Ar- thritis Rheum 1991;34:393-402. 31. Akin E, McHugh GL, Flavell RA, Fikrig E, Steere AC. The immuno- globin (IgG) antibody response to OspA and OspB correlates with severe and prolonged Lyme arthritis and the IgG response to P35 correlates with mild and brief arthritis. Infect Immun 1999;67:173-81. 32. Asbrink E, Hovmark A. Successful cultivation of spirochetes from skin lesions of patients with erythema chronicum migrans Afzelius and acroder- matitis chronica atrophicans. Acta Pathol Microbiol Immunol Scand [B] 1985;93:161-3. 33. Brown EL, Rivas JM, Ullrich SE, Young CR, Norris SJ, Kripke ML. STEERE · 9
Modulation of immunity to Borrelia burgdorferi by ultraviolet irradiation: differential effect on Th1 and Th2 immune responses. Eur J Immunol 1995;25:3017-22. 34. Coyle PK, Goodman JL, Krupp LB, Logigian EL, Reik L Jr. Lyme disease: continuum: lifelong learning in neurology. Vol. 5. No. 4. Part A. Philadelphia: Lippincott Williams & Wilkins, August 1999. 35. Oschmann P, Dorndorf W, Hornig C, Schafer C, Wellensiek HJ, Pflughaupt KW. Stages and syndromes of neuroborreliosis. J Neurol 1998; 245:262-72. 36. Rothermel H, Hedges TR III, Steere AC. Optic neuropathy in chil- dren with Lyme disease. Pediatrics (in press). 37. Roberts ED, Bohm RP Jr, Lowrie RC Jr, et al. Pathogenesis of Lyme neuroborreliosis in the rhesus monkey: the early disseminated and chronic phases of disease in the peripheral nervous system. J Infect Dis 1998;178: 722-32. 38. Cadavid D, O’Neill T, Schaefer H, Pachner AR. Localization of Bor- relia burgdorferi in the nervous system and other organs in a nonhuman primate model of Lyme disease. Lab Invest 2000;80:1043-54. 39. Logigian EL, Kaplan RF, Steere AC. Chronic neurologic manifesta- tions of Lyme disease. N Engl J Med 1990;323:1438-44. 40. Logigian EL, Steere AC. Clinical and electrophysiologic findings in chronic neuropathy of Lyme disease. Neurology 1992;42:303-11. 41. Halperin JJ, Luft BJ, Anand AK, et al. Lyme neuroborreliosis: central nervous system manifestations. Neurology 1989;39:753-9. 42. Logigian EL, Kaplan RF, Steere AC. Successful treatment of Lyme en- cephalopathy with intravenous ceftriaxone. J Infect Dis 1999;180:377-83. 43. Hemmer B, Gran B, Zhao Y, et al. Identification of candidate T-cell epitopes and molecular mimics in chronic Lyme disease. Nat Med 1999;5: 1375-82. 44. Kelleher Doyle M, Telford SR III, Criscione L, Lin SR, Spielman A, Gravallese EM. Cytokines in murine Lyme carditis: Th1 cytokine expres- sion follows expression of proinflammatory cytokines in a susceptible mouse strain. J Infect Dis 1998;177:242-6. 45. Barthold SW, Feng S, Bockenstedt LK, Fikrig E, Feen K. Protective and arthritis-resolving activity in sera of mice infected with Borrelia burg- dorferi. Clin Infect Dis 1997;25:Suppl 1:S9-S17. 46. Stanek G, Klein J, Bittner R, Glogar D. Isolation of Borrelia burgdor- feri from the myocardium of a patient with longstanding cardiomyopathy. N Engl J Med 1990;322:249-52. 47. Lardieri G, Salvi A, Camerini F, Cinco M, Trevisan G. Isolation of Bor- relia burgdorferi from myocardium. Lancet 1993;342:490. 48. Sonnesyn SW, Diehl SC, Johnson RC, Kubo SH, Goodman JL. A prospective study of the seroprevalance of Borrelia burgdorferi infection in patients with severe heart failure. Am J Cardiol 1995;76:97-100. 49. Steere AC, Duray PH, Butcher EC. Spirochetal antigens and lymphoid cell surface markers in Lyme synovitis: comparison with rheumatoid syn- ovium and tonsillar lymphoid tissue. Arthritis Rheum 1988;31:487-95. 50. Vincent MS, Roessner K, Sellati T, et al. Lyme arthritis synovial gd T cells respond to Borrelia burgdorferi lipoproteins and lipidated hexapep- tides. J Immunol 1998;161:5762-71. 51. Chen J, Field JA, Glickstein L, Molloy PJ, Huber BT, Steere AC. As- sociation of antibiotic treatment-resistant Lyme arthritis with T cell re- sponses to dominant epitopes of outer surface protein A of Borrelia burg- dorferi. Arthritis Rheum 1999;42:1813-22. 52. Gross DM, Steere AC, Huber BT. T helper 1 response is dominant and localized to the synovial fluid in patients with Lyme arthritis. J Immunol 1998;160:1022-8. 53. Yin Z, Braun J, Neure L, et al. T cell cytokine pattern in the joints of patients with Lyme arthritis and its regulation by cytokines and anticyto- kines. Arthritis Rheum 1997;40:69-79. 54. Dressler F, Whalen JA, Reinhardt BN, Steere AC. Western blotting in the serodiagnosis of Lyme disease. J Infect Dis 1993;167:392-400. 55. Barthold SW, Beck DS, Hansen GM, Terwilliger GA, Moody KD. Lyme borreliosis in selected strains and ages of laboratory mice. J Infect Dis 1990;162:133-8. 56. Feng S, Hodzic E, Barthold SW. Lyme arthritis resolution with anti- serum to a 37-kilodalton Borrelia burgdorferi protein. Infect Immun 2000; 68:4169-73. 57. Steere AC, Baxter-Lowe LA. Association of chronic, treatment-resist- ant Lyme arthritis with rheumatoid arthritis (RA) alleles. Arthritis Rheum 1998;41:Suppl:S81. abstract. 58. Steere AC, Levin RE, Molloy PJ, et al. Treatment of Lyme arthritis. Arthritis Rheum 1994;37:878-88. 59. Nocton JJ, Dressler F, Rutledge BJ, Rys PN, Persing DH, Steere AC. Detection of Borrelia burgdorferi DNA by polymerase chain reaction in synovial fluid from patients with Lyme arthritis. N Engl J Med 1994;330: 229-34. 60. Carlson D, Hernandez J, Bloom BJ, Coburn J, Aversa JM, Steere AC. Lack of Borrelia burgdorferi DNA in synovial samples in patients with an- tibiotic treatment-resistant Lyme arthritis. Arthritis Rheum 1999;42: 2705-9. 61. Kalish RA, Leong JM, Steere AC. Association of treatment-resistant chronic Lyme arthritis with HLA-DR4 and antibody reactivity to OspA and OspB of Borrelia burgdorferi. Infect Immun 1993;61:2774-9. 62. Gross DM, Forsthuber T, Tary-Lehmann M, et al. Identification of LFA-1 as a candidate autoantigen in treatment-resistant Lyme arthritis. Sci- ence 1998;281:703-6. 63. Meyer AL, Trollmo C, Crawford F, et al. Direct enumeration of Bor- relia-reactive CD4+ T cells ex vivo by using MHC class II tetramers. Proc Natl Acad Sci U S A 2000;97:11433-8. 64. Trollmo C, Meyer AL, Steere AC, Hafler DA, Huber BT. Molecular mimicry in Lyme arthritis demonstrated at the single cell level: LFA-1a is a partial agonist for outer surface protein A-reactive T cells. J Immunol 2001;166:5286-91. 65. Berger BW, Johnson RC, Kodner C, Coleman L. Cultivation of Bor- relia burgdorferi from erythema migrans lesions and perilesional skin. J Clin Microbiol 1992;30:359-61. 66. Nocton JJ, Bloom BJ, Rutledge BJ, et al. Detection of Borrelia burg- dorferi DNA by polymerase chain reaction in cerebrospinal fluid in patients with Lyme neuroborreliosis. J Infect Dis 1996;174:623-7. 67. Klempner MS, Schmid C, Hu L, et al. Intralaboratory reliability of se- rologic and urine testing for Lyme disease. Am J Med 2001;110:217-9. 68. Case definitions for public health surveillance. MMWR Morb Mortal Wkly Rep 1990;39(RR-13):1-43. 69. Recommendations for test performance and interpretation from the Second National Conference on Serologic Diagnosis of Lyme Disease. MMWR Morb Mortal Wkly Rep 1995;44:590-1. 70. Robertson J, Guy E, Andrews N, et al. A European multicenter study of immunoblotting in serodiagnosis of Lyme borreliosis. J Clin Microbiol 2000;38:2097-102. 71. Engstrom SM, Shoop E, Johnson RC. Immunoblot interpretation cri- teria for serodiagnosis of early Lyme disease. J Clin Microbiol 1995;33: 419-27. 72. Steere AC, Berardi VP, Weeks KE, Logigian EL, Ackermann R. Eval- uation of the intrathecal antibody response to Borrelia burgdorferi as a di- agnostic test for Lyme neuroborreliosis. J Infect Dis 1990;161:1203-9. 73. Kalish RA, McHugh G, Granquist J, Shea B, Ruthazer R, Steere AC. Persistence of IgM or IgG antibody responses to Borrelia burgdorferi 10 to 20 years after active Lyme disease. Clin Infect Dis (in press). 74. Steere AC, Sikand VK, Meurice F, et al. Vaccination against Lyme dis- ease with recombinant Borrelia burgdorferi outer-surface lipoprotein A with adjuvant. N Engl J Med 1998;339:209-15. 75. Gustafson R, Svenungsson B, Gardulf A, Stiernstedt G, Forsgren M. Prevalence of tick-borne encephalitis and Lyme borreliosis in a defined Swedish population. Scand J Infect Dis 1990;22:297-306. 76. Gomes-Solecki MJ, Dunn JJ, Luft BJ, et al. Recombinant chimeric Borrelia proteins for diagnosis of Lyme disease. J Clin Microbiol 2000;38: 2530-5. 77. Liang FT, Steere AC, Marques AR, Johnson BJ, Miller JN, Philipp MT. Sensitive and specific serodiagnosis of Lyme disease by enzyme-linked immu- nosorbent assay with a peptide based on an immunodominant conserved re- gion of Borrelia burgdorferi vlsE. J Clin Microbiol 1999;37:3990-6. 78. Wormser GP, Nadelman RB, Dattwyler RJ, et al. Practice guidelines for the treatment of Lyme disease. Clin Infect Dis 2000;31:Suppl 1:S1-S14. 79. Nichol G, Dennis DT, Steere AC, et al. Test-treatment strategies for patients suspected of having Lyme disease: a cost-effectiveness analysis. Ann Intern Med 1998;128:37-48. 80. Recommendations for the use of Lyme disease vaccine: recommenda- tions of the Advisory Committee on Immunization Practices (ACIP). MMWR Morb Mortal Wkly Rep 1999;48(RR-7):1-17, 21-5. [Erratum, MMWR Morb Mortal Wkly Rep 1999;48:833.] 81. Williams CL, Stobino B, Weinstein A, Spierling P, Medici F. Maternal Lyme disease and congenital malformations: a cord blood serosurvey in en- demic and control areas. Paediatr Perinat Epidemiol 1995;9:320-30. 82. Dattwyler RJ, Volkman DJ, Conaty SM, Platkin SP, Luft BJ. Amoxy- cillin plus probenecid versus doxycycline for treatment of erythema migrans borreliosis. Lancet 1990;336:1404-6. 83. Nadelman RB, Luger SW, Frank E, Wisniewski M, Collins JJ, Worm- ser GP. Comparison of cefuroxime axetil and doxycycline in the treatment of early Lyme disease. Ann Intern Med 1992;117:273-80. 84. Dattwyler RJ, Luft BJ, Kunkel MJ, et al. Ceftriaxone compared with doxycycline for the treatment of acute disseminated Lyme disease. N Engl J Med 1997;337:289-94. 85. Nowakowski J, McKenna D, Nadelman RB, et al. Failure of treatment with cephalexin for Lyme disease. Arch Fam Med 2000;9:563-7. 86. Dattwyler RJ, Halperin JJ, Volkman DJ, Luft BJ. Treatment of late Lyme borreliosis — randomised comparison of ceftriaxone and penicillin. Lancet 1988;1:1191-4. 10 · STEERE The New England Journal of Medicine
87. Pfister HW, Preac-Mursic V, Wilske B, Einhaupl KM. Cefotaxime vs penicillin G for acute neurologic manifestations of Lyme borreliosis: a pro- spective randomized study. Arch Neurol 1989;46:1190-4. 88. Karlsson M, Hammers-Berggren S, Lindquist L, Stiernstedt G, Sven- ungsson B. Comparison of intravenous penicillin G and oral doxycycline for treatment of Lyme neuroborreliosis. Neurology 1994;44:1203-7. 89. Eckman MH, Steere AC, Kalish RA, Pauker SG. Cost effectiveness of oral as compared with intravenous antibiotic therapy for patients with early Lyme disease or Lyme arthritis. N Engl J Med 1997;337:357-63. 90. Dinerman H, Steere AC. Lyme disease associated with fibromyalgia. Ann Intern Med 1992;117:281-5. 91. Shadick NA, Phillips CB, Sangha O, et al. Musculoskeletal and neuro- logic outcomes in patients with previously treated Lyme disease. Ann In- tern Med 1999;131:919-26. 92. Kalish RA, Kaplan RF, Taylor E, Jones-Woodward L, Workman K, Steere AC. Evaluation of study patients with Lyme disease, 10-20-year fol- low-up. J Infect Dis 2001;183:453-60. 93. Seltzer EG, Gerber MA, Cartter ML, Freudigman K, Shapiro ED. Long- term outcomes of persons with Lyme disease. JAMA 2000;283:609-16. 94. Klempner MS, Hu LT, Evans J, et al. Two controlled trials of antibiotic treatment in patients with persistent symptoms and a history of Lyme dis- ease. N Engl J Med 2001;345:xxx-xx. 95. Ettestad PJ, Campbell GL, Welbel SF, et al. Biliary complications in the treatment of unsubstantiated Lyme disease. J Infect Dis 1995;171:356- 61. 96. Patel R, Grogg KL, Edwards WD, Wright AJ, Schwenk NM. Death from inappropriate therapy for Lyme disease. Clin Infect Dis 2000;31: 1107-9. 97. Shapiro ED, Gerber MA, Holabird NB, et al. A controlled trial of an- timicrobial prophylaxis for Lyme disease after deer-tick bites. N Engl J Med 1992;327:1769-73. 98. Piesman J. Dynamics of Borrelia burgdorferi transmission by nymphal Ixodes dammini ticks. J Infect Dis 1993;167:1082-5. 99. Nadelman RB, Nowakowski J, Fish D, et al. Prophylaxis with single- dose doxycycline for the prevention of Lyme disease after an Ixodes scapularis tick bite. N Engl J Med 2001;345:xxx-xx. 100. Schoen RT, Sikand VK, Caldwell MC, et al. Safety and immunoge- nicity profile of a recombinant outer-surface protein A Lyme disease vac- cine: clinical trial of a 3-dose schedule at 0, 1, and 2 months. Clin Ther 2000;22:315-25.


From the Division of Rheumatology and Immunology, Tufts University School of Medicine, Boston. Address reprint requests to Dr. Steere at the Division of Rheumatology and Immunology, New England Medical Cen- ter #406, 750 Washington St., Boston, MA 02111.



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