Overview
Brill-Zinsser disease (also known as recrudescent typhus or recrudescent epidemic typhus) is a relapse form of epidemic typhus caused by the bacterium Rickettsia prowazekii. It occurs years or even decades after an initial episode of epidemic typhus, when dormant organisms reactivate in a person whose immunity has waned due to aging, stress, malnutrition, or immunosuppression. Unlike the original epidemic typhus, which is transmitted by body lice, Brill-Zinsser disease arises endogenously from persistent rickettsial organisms harbored in the patient's own tissues, though an affected individual can serve as a source of infection to lice and thereby spark new outbreaks of epidemic typhus in susceptible populations. The disease primarily affects the vascular system, as Rickettsia prowazekii targets endothelial cells lining blood vessels, leading to widespread vasculitis. Key clinical features include sudden onset of fever, severe headache, myalgia (muscle pain), and a maculopapular rash that typically begins on the trunk and spreads to the extremities. Neurological symptoms such as confusion and delirium may occur. Compared to primary epidemic typhus, Brill-Zinsser disease tends to be milder and shorter in duration, with lower mortality rates, partly because of residual partial immunity from the initial infection. Diagnosis is based on clinical suspicion, a history of prior epidemic typhus exposure, and serological testing. Notably, the antibody response in Brill-Zinsser disease is predominantly IgG (an anamnestic response), in contrast to the IgM-predominant response seen in primary infection. Treatment consists of antibiotic therapy, with doxycycline being the drug of choice. Chloramphenicol is an alternative. With appropriate antibiotic treatment, prognosis is generally excellent, and most patients recover fully. Without treatment, mortality is estimated at around 1-2%, significantly lower than untreated primary epidemic typhus.
Also known as:
Adult
Begins in adulthood (age 18 or older)
FDA & Trial Timeline
1 eventLao-Oxford-Mahosot Hospital Wellcome Trust Research Unit — PHASE2, PHASE3
Data sourced from FDA regulatory filings and ClinicalTrials.gov. Updated periodically.
Treatments
No FDA-approved treatments are currently listed for Brill-Zinsser disease.
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Treatment Centers
8 centersBaylor College of Medicine Rare Disease Center ↗
Baylor College of Medicine
📍 Houston, TX
🏥 NORDStanford Medicine Rare Disease Center ↗
Stanford Medicine
📍 Stanford, CA
🔬 UDNNIH Clinical Center Undiagnosed Diseases Program ↗
National Institutes of Health
📍 Bethesda, MD
🔬 UDNUCLA UDN Clinical Site ↗
UCLA Health
📍 Los Angeles, CA
🔬 UDNBaylor College of Medicine UDN Clinical Site ↗
Baylor College of Medicine
📍 Houston, TX
🔬 UDNHarvard/MGH UDN Clinical Site ↗
Massachusetts General Hospital
📍 Boston, MA
🏥 NORDMayo Clinic Center for Individualized Medicine ↗
Mayo Clinic
📍 Rochester, MN
👤 Mayo Clinic Center for Individualized Medicine
🏥 NORDUCLA Rare Disease Day Program ↗
UCLA Health
📍 Los Angeles, CA
Travel Grants
No travel grants are currently matched to Brill-Zinsser disease.
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Disease timeline:
New recruiting trial: QuEST - Quick and Easy Scrub Typhus Diagnostic Tools
A new clinical trial is recruiting patients for Brill-Zinsser disease
New recruiting trial: Scrub Typhus Antibiotic Resistance Trial
A new clinical trial is recruiting patients for Brill-Zinsser disease
New recruiting trial: Rickettsia Clearance Study
A new clinical trial is recruiting patients for Brill-Zinsser disease
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Common questions about Brill-Zinsser disease
What is Brill-Zinsser disease?
Brill-Zinsser disease (also known as recrudescent typhus or recrudescent epidemic typhus) is a relapse form of epidemic typhus caused by the bacterium Rickettsia prowazekii. It occurs years or even decades after an initial episode of epidemic typhus, when dormant organisms reactivate in a person whose immunity has waned due to aging, stress, malnutrition, or immunosuppression. Unlike the original epidemic typhus, which is transmitted by body lice, Brill-Zinsser disease arises endogenously from persistent rickettsial organisms harbored in the patient's own tissues, though an affected individual
At what age does Brill-Zinsser disease typically begin?
Typical onset of Brill-Zinsser disease is adult. Age of onset can vary across affected individuals.
Which specialists treat Brill-Zinsser disease?
8 specialists and care centers treating Brill-Zinsser disease are listed on UniteRare, sourced from ClinicalTrials.gov principal investigators, published research, and the NPPES NPI registry.