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Volume 6, Number 6—December 2000


Meningococcemia in a Patient Coinfected with Hepatitis C Virus and HIV

Christopher G. Nelson, Mark A. Iler, Christopher W. Woods, John A. Bartlett, and Vance G. FowlerComments to Author 
Author affiliations: Duke University Medical Center, Durham, North Carolina, USA

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EID Nelson CG, Iler MA, Woods CW, Bartlett JA, Fowler VG. Meningococcemia in a Patient Coinfected with Hepatitis C Virus and HIV. Emerg Infect Dis. 2000;6(6):646-648.
AMA Nelson CG, Iler MA, Woods CW, et al. Meningococcemia in a Patient Coinfected with Hepatitis C Virus and HIV. Emerging Infectious Diseases. 2000;6(6):646-648. doi:10.3201/eid0606.000615.
APA Nelson, C. G., Iler, M. A., Woods, C. W., Bartlett, J. A., & Fowler, V. G. (2000). Meningococcemia in a Patient Coinfected with Hepatitis C Virus and HIV. Emerging Infectious Diseases, 6(6), 646-648.


Coinfection with hepatitis C virus (HCV) and HIV is an emerging public health problem. While coinfection with HIV can accelerate the progression of HCV (1,2), the impact of dual infection on other infectious diseases is unknown. We describe the first reported case of meningococcal infection in a patient coinfected with HCV and HIV.

Case Report

A 45-year-old woman was admitted to our hospital emergency department in September 1999 with influenza-like symptoms (36 hours) and fever, headache, and myalgias (12 hours). The patient's medical history included ongoing injection drug use, coinfection with HIV and HCV, an episode of Staphylocccus aureus cervical osteomyelitis, three culture-confirmed episodes of Streptococcus pneumoniae pneumonia, and HIV-associated thrombocytopenia. Her most recent CD4 count was 149 cells/microliter, and in April 1999, her plasma HIV RNA level was 2,000 viral copies per microliter. She had received pneumococcal polysaccharide vaccine in 1996. Because of ongoing injection drug use, she had never received antiretroviral therapy. Her medications included trimethoprim/sulfamethoxazole, paroxetine, nifedipine, furosemide, and methadone.

The patient was lethargic (oral temperature 40.3°C, blood pressure 82/45 mm Hg, pulse rate 100 beats per minute, and respiratory rate 24 breaths per minute). Physical examination showed meningismus, bilateral conjunctival hemorrhages, diffuse petechiae, and tender palpable purpura on the lower extremities. Neurologic examination was nonfocal. Initial laboratory findings were as follows: hematocrit, 46%; platelet count, 69 x 109/L; leukocyte count, 6.0 x 109/L; creatinine, 1.6 mg/dL; aspartate aminotransferase,61 U/L; alanine aminotransferase, 28 U/L; total bilirubin, 0.8 mg/L; alkaline phosphatase, 96 U/L; prothrombin time/international normalized ratio,14.1 seconds/1.3; partial thromboplastin time, 29.4 seconds. Urinalysis showed 14 red blood cells and 28 leukocytes per high-power field, no casts, and 3+ proteinuria. A later urinalysis showed that both the proteinuria and cellular elements had resolved. No schistocytes were visible on peripheral blood smear. A skin lesion biopsy performed in the emergency room revealed a thrombotic vasculopathy without evidence of rickettsiae (by direct immunoflourescence) or other microorganisms.

Because of concern for possible bacterial meningitis, the patient was immediately given 2 g ceftriaxone intravenously. After computed tomography of the brain revealed no acute intracranial process, lumbar puncture was performed. The cerebrospinal fluid was cloudy, with 7,675 nucleated cells/mm (92% neutrophils and 3% band forms). Protein was 382 mg/dL, and glucose was less than 20 mg/dL. Gram stain showed 3+ gram-negative diplococci. Cultures of the cerebrospinal fluid and blood yielded pure growth of serogroup Y Neisseria meningitidis.

The patient received a 10-day course of intravenous ceftriaxone, 2 g every 12 hrs. Whole hemolytic complement (CH50) drawn on hospital day 5 was 13 units (23-52 units). Other complement assays included a C3 value of 105 mg/dL (86-208 mg/dL) and a C4 value of 8 mg/dL (13-47 mg/dL. Results of a cryoglobulin screen were positive. Computed tomography of the abdomen revealed nodular liver and splenomegaly consistent with cirrhosis. The patient was given meningococcal vaccine near the end of her hospital course and was discharged with no sequelae. On followup with her primary physician, she had no evidence of complications from the meningococcemia. A repeat CH50 drawn 6 months after hospitalization was <10 units (23-52 units).


To our knowledge this is the first reported case of disseminated meningococcemia in a patient coinfected with HIV and HCV. Because coinfected patients constitute an increasing percentage of patients infected with HIV (2), several features of this case bear emphasis.

First, hepatic dysfunction from conditions such as HCV is an important risk factor for meningococcal disease (3). This increased risk is likely due to decreased hepatic synthesis of complement (3). Because hypocomplementemia occurs commonly in patients infected with HCV, particularly when cirrhosis or cryoglobulinemia is present (4), these patients are at increased risk for meningococcal infection (3). Patients who are coinfected with HIV and HCV may be at even greater risk for meningococcal infection because of accelerated hepatic destruction. For example, patients coinfected with HIV and HCV have a higher progression to hepatic fibrosis (1) and a 3.5-fold increase in hepatic cirrhosis (2), when compared to patients with HCV alone. Given that up to 9% of HIV-infected patients may be coinfected with HCV (2), a group of patients with potentially increased susceptibility to meningococcal infection may be emerging.

Second, unlike the interaction between HIV and S. pneumoniae, Salmonella, and other recognized bacterial opportunistic pathogens, the interaction between HIV and meningococcus is unclear. Less than 50 cases of meningococcal infections in HIV-infected patients have been reported in PUBMED (5-14). These reports present conflicting results on the impact of HIV infection on the risk for meningococcal disease. For example, while one recent prospective cohort study reported an increased risk for meningococcal disease (RR 23.8, CI 7.4-76.7; p <0.001) in HIV-infected patients in the Atlanta metropolitan area (12), a case-control study in Africa showed no link between HIV infection and epidemic meningococcal disease (14). Despite the low rate of reported infection, asymptomatic colonization with meningococcus occurs in as many as 15%-23% of tested cohorts of both HIV-infected patients (15) and healthy young adults (16).

There are limitations to our report. Because our patient had several pneumococcal infections before the meningococcemia, immunologic defects other than hypocomplementemia (such as advanced HIV) may have contributed to susceptibility to both of these bacterial pathogens. Only limited data may be inferred from a single case. For example, assuming that the overall rate of meningococcal disease in the United States is 1/100,000, that 1% of the U.S. population is HIV positive, and that 9% of these patients are coinfected with HCV, only two to three cases of meningococcal infection would be expected to occur among coinfected patients if no additional risk for meningococcal infection were present. Because the true incidence of meningococcal infection among coinfected patients is unknown, future cohort studies will have to establish the impact of coinfection with HIV and HCV on the risk for meningococcal infection.

Dr. Nelson is a third-year resident in the Department of Internal Medicine at Duke University Medical Center, Durham, North Carolina. He has a DVM degree from the School of Veterinary Medicine at University of California Davis. His research interests include pulmonary and critical care medicine as well as zoonotic diseases.


This study was supported by National Institutes of Health grant AI-01647.


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Cite This Article

DOI: 10.3201/eid0606.000615

Table of Contents – Volume 6, Number 6—December 2000


Please use the form below to submit correspondence to the authors or contact them at the following address:

Vance G. Fowler, Jr., Box 3281, Division of Infectious Diseases, Duke University Medical Center, Durham, NC 27710 USA; fax:919-684-8902

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