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Impaired Antibody Response to Pneumococcal Vaccine after Treatment for Hodgkin's Disease

List of authors.
  • George R. Siber, M.D.,
  • Sigmund A. Weitzman, M.D.,
  • Alan C. Aisenberg, M.D., Ph.D.,
  • Howard J. Weinstein, M.D.,
  • and Gerald Schiffman, Ph.D.

Abstract

To determine if a normal antibody response can develop after therapy for Hodgkin's disease, we immunized 53 patients and 10 normal controls with dodecavalent pneumococcal vaccine. Antibody concentrations three weeks after immunization (geometric mean of 11 serotypes) were 1566 ng of protein nitrogen per milliliter in controls, 963 ng per milliliter after subtotal radiation (P<0.05 compared to controls), 658 ng per milliliter after chemotherapy (P<0.05), 377 ng per milliliter after subtotal radiation plus chemotherapy (P<0.01) and 283 ng per milliliter after total nodal radiation plus chemotherapy (P<0.001). Low levels of antibody before immunization correlated with a poor response (r = +0.73, P<0.001). The ability to respond to immunization improved significantly but did not return to normal as long as four years after combined therapy. The antibody response to pneumococcal vaccine is profoundly impaired in patients who have received intensive treatment for Hodgkin's disease: the ability of this vaccine to protect them from overwhelming postsplenectomy infections remains in doubt. (N Engl J Med 299:442–448, 1978)

Funding and Disclosures

Supported by grants from the American Cancer Society (RD23) and from the National Institutes of Health (RR 01032 and N0 AI 42541).

We are indebted to Mary Ellen Shea, R.N., Marlyne Morrow, R.N., Peter Skapriwsky, Joan Boudreault, Ray Castagna, and Chand Dham for technical assistance, to Drs. Robert Carey, Zareh Demirjian, Sheldon Kaufman, Rita Kelley and W. D. Sohier, Jr., for providing patients for study and to Bernard Ransil, M.D., and Kenneth E. Stanley, Ph.D., for advice on data analysis.

Author Affiliations

From the Department of Clinical Microbiology, Sidney Farber Cancer Institute, the Medical Oncology Unit, Department of Medicine and the Huntington Laboratories of the Massachusetts General Hospital and the Department of Microbiology and Immunology, State University of New York, Downstate Medical Center (address reprint requests to Dr. Siber at the Sidney Farber Cancer Institute, 44 Binney St., Boston, MA 02115).

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