Volume 25, Number 4—April 2019
Combination of Clindamycin and Azithromycin as Alternative Treatment for Toxoplasma gondii Encephalitis
Current standard therapies for toxoplasmic encephalitis often cause severe adverse events. A 57-year-old HIV-positive man in Japan who had toxoplasmic encephalitis but was intolerant to trimethoprim/sulfamethoxazole, pyrimethamine, sulfadiazine, and atovaquone was successfully treated with the combination of clindamycin and azithromycin. This drug combination can be an alternative treatment for this condition.
Current treatment guidelines for toxoplasmic encephalitis (TE) (1) recommend either pyrimethamine plus sulfadiazine or pyrimethamine plus clindamycin; trimethoprim/sulfamethoxazole is also known to have comparable potency (2). However, kidney, liver, and hematologic toxicity, as well as hypersensitivities, often have been reported (2), and few alternatives are available. We report a TE patient who experienced severe toxicity after all standard regimens but was successfully treated with a combination of clindamycin and azithromycin.
A 57-year-old man sought care at the National Centre for Global Health and Medicine (Tokyo, Japan) with fever and mild disorientation. On examination, he was febrile and drowsy with slurred speech. He did not exhibit any apparent focal neurologic deficits.
Blood laboratory test results (reference ranges) were as follows: hemoglobin, 10.4 g/dL (13.7–16.8 g/dL); total leukocyte count, 6.81 × 103 cells/L (3.3–8.6 × 103 cells/L); platelet count, 2.43 × 105/L (1.58–3.48 × 105/L); β-
Trimethoprim/sulfamethoxazole (10 mg/kg/d trimethoprim) was first initiated because of limited availability of pyrimethamine plus sulfadiazine at the time, but acute liver toxicity developed on treatment day 6 (increases in levels of aminotransferase/alanine aminotransferase from 24/20 IU/L to 127/145 IU/L[(reference 10–42 IU/L]). Pyrimethamine plus sulfadiazine was started on treatment day 7. However, on day 9, acute renal failure developed because of obstructive urolithiasis caused by sulfadiazine crystals. After the patient was switched to pyrimethamine plus clindamycin, his renal function persistently worsened, and a drug-induced lymphocyte stimulation test suggested that pyrimethamine was responsible for the acute renal failure. A switch to atovaquone on treatment day 12 resulted in thrombocytopenia by day 17.
After switching to the combination of clindamycin (2,400 mg/d) and azithromycin (1,200 mg/d), the patient did not experience any apparent adverse effects or show abnormal laboratory values. He successfully started antiretroviral therapy for his HIV infection during week 6. Repeated brain magnetic resonance imaging performed 1, 3, and 8 months after presentation showed all lesions had substantially decreased, and only a residual nonenhancing lesion was observed 12 months after presentation (Figure, panels B–D). The patient has continued maintenance therapy with the same dose of clindamycin and azithromycin without any symptoms of relapse or immune reconstitution inflammatory syndrome.
Several reports have documented the high prevalence of various adverse events associated with the aforementioned standard therapies for TE (2,4), but little information is available regarding the efficacy of alternative drugs. Although atovaquone is the only safe alternative agent for which efficacy and safety have been relatively well established, it has been proven to be less potent than standard therapies (5).
Clindamycin has in vitro activity against Toxoplasma gondii, inhibitory effects in vivo at lower concentrations (6), and the ability to penetrate into CSF (7), suggesting that it is a promising alternative agent for TE treatment. More important, clindamycin causes far fewer adverse events than sulfadiazine (2,4). Although the potency of clindamycin monotherapy has not been assessed, some case reports suggested its effectiveness (8). Therefore, a clindamycin-containing combination with potent agents other than pyrimethamine may be a reasonable treatment option for TE treatment.
Macrolides also have displayed substantial in vitro efficacy against T. gondii (9). A phase I/II dose-escalation study of oral azithromycin in combination with pyrimethamine revealed the relative efficacy and safety of the regimen (10). Azithromycin combined with a potent agent other than pyrimethamine, such as clindamycin, can be theoretically expected to be a safe and effective option. Further study should be conducted to establish safer treatment options for TE.
The continuous reduction in the size of the lesion in the patient we report was partly explained by his good immune recovery. Our results suggest that the combination of clindamycin and macrolides could be a safer and potent alternative therapy for patients who are intolerant of current standard regimens.
Dr. Shiojiri is a fellow at the AIDS Clinical Centre, National Centre for Global Health and Medicine, Tokyo, Japan. His primary research interests include anal human papillomavirus infection and anal precancer among men who have sex with men in Japan.
We thank Tokio Hoshina for detecting Toxoplasma nucleic acid by LAMP.
- US Department of Health and Human Serivces. Guidelines for the prevention and treatment of opportunistic infections in HIV-infected adults and adolescents [cited 2018 Aug 23]. https://aidsinfo.nih.gov/guidelines
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Original Publication Date: February 28, 2019
Table of Contents – Volume 25, Number 4—April 2019
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Daisuke Shiojiri, AIDS Clinical Centre, National Centre for Global Health and Medicine, 1-21-1, Toyama, Shinjuku-ku, Tokyo 192-8655, Japan