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Published on: November 5, 2019
Nosocomial aseptic meningitis associated with administration of OKT3
M A Martin1, R M Massanari, D D Nghiem
1Department of Medicine, University of Iowa College of Medicine, Iowa City.
Abstract:
An outbreak of nosocomial aseptic meningitis involving four renal allograft recipients on the transplant service occurred in July 1986, shortly after the release of the murine monoclonal antibody OKT3 for therapy for acute allograft rejection. No bacteria, fungi, or viruses were isolated from cultures of the cerebrospinal fluid of the four patients. All four had acute allograft rejection treated with OKT3 and developed signs and/or symptoms of meningitis within 72 hours of receiving the drug. To identify potential risk factors, the four patients with aseptic meningitis were compared with 12 patients on the renal transplant service in July 1986 who did not have signs or symptoms of meningitis. The development of aseptic meningitis was strongly associated with administration of OKT3. Because of this association, prospective surveillance of meningitis in patients receiving OKT3 was instituted. From November 1986 to May 1987, three (14%) of 21 patients treated with OKT3 developed aseptic meningitis. The clinical course of aseptic meningitis associated with OKT3 appears to be benign and self-limited. Nonetheless, this observation warrants continued surveillance of OKT3 therapy.
Insights
Aseptic meningitis occurred in renal transplant patients treated with the murine monoclonal antibody OKT3 (muromonab-CD3) for acute allograft rejection. This condition was strongly associated with OKT3 administration and appeared to be self-limiting.
Area of Science:
- Nephrology
- Immunology
- Infectious Diseases
Background:
- Nosocomial aseptic meningitis is a rare complication in immunocompromised patients.
- The murine monoclonal antibody OKT3 (muromonab-CD3) is used to treat acute renal allograft rejection.
- An outbreak of meningitis was observed in renal transplant recipients.
Purpose of the Study:
- To investigate an outbreak of aseptic meningitis in renal allograft recipients.
- To identify potential risk factors for meningitis in transplant patients.
- To determine the association between OKT3 therapy and aseptic meningitis.
Main Methods:
- Retrospective case-control study comparing patients with and without meningitis.
- Cerebrospinal fluid cultures were performed to rule out infectious causes.
- Prospective surveillance of meningitis in patients receiving OKT3 was implemented.
Main Results:
- Four renal allograft recipients developed aseptic meningitis within 72 hours of OKT3 administration.
- No infectious agents were isolated from cerebrospinal fluid.
- Aseptic meningitis was strongly associated with OKT3 treatment.
- Prospective surveillance identified 3 cases (14%) of aseptic meningitis in 21 patients treated with OKT3.
Conclusions:
- Administration of OKT3 is strongly associated with the development of aseptic meningitis in renal transplant recipients.
- The clinical course of OKT3-associated aseptic meningitis appears benign and self-limited.
- Continued surveillance of OKT3 therapy for meningitis is warranted.
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