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Use of Cytomegalovirus Immune Globulin to Prevent Cytomegalovirus Disease in Renal-Transplant Recipients

List of authors.
  • David R. Snydman, M.D.,
  • Barbara G. Werner, Ph.D.,
  • Beverly Heinze-Lacey, R.N., M.P.H.,
  • Victor P. Berardi,
  • Nicholas L. Tilney, M.D.,
  • Robert L. Kirkman, M.D.,
  • Edgar L. Milford, M.D.,
  • Sang I. Cho, M.D.,
  • Harry L. Bush, Jr., M.D.,
  • Andrew S. Levey, M.D.,
  • Terry B. Strom, M.D.,
  • Charles B. Carpenter, M.D.,
  • Raphael H. Levey, M.D.,
  • William E. Harmon, M.D.,
  • Clarence E. Zimmerman, II, M.D.,
  • Michael E. Shapiro, M.D.,
  • Theodore Steinman, M.D.,
  • Frank LoGerfo, M.D.,
  • Beldon Idelson, M.D.,
  • Gerhard P.J. Schröter, M.D.,
  • Myron J. Levin, M.D.,
  • James McIver, Ph.D.,
  • Jeanne Leszczynski, DR.P.H.,
  • and George F. Grady, M.D.

Abstract

We undertook a prospective randomized trial to examine whether an intravenous cytomegalovirus (CMV) immune globulin would prevent primary CMV disease in renal-transplant recipients. Fifty-nine CMV-seronegative patients who received kidneys from donors who had antibodies against CMV were assigned to receive either intravenous CMV immune globulin or no treatment. The immune globulin was administered in multiple doses over the first four months after transplantation.

The incidence of virologically confirmed CMV-associated syndromes was reduced from 60 percent in controls to 21 percent in recipients of CMV immune globulin (P<0.01). Fungal or parasitic superinfections were not seen in globulin recipients but occurred in 20 percent of controls (P = 0.05). Only 4 percent of globulin recipients had marked leukopenia (reflecting serious CMV disease), as compared with 37 percent of the controls (P<0.01). There was a concomitant but not statistically significant reduction in the incidence of CMV pneumonia (17 percent of controls as compared with 4 percent of globulin recipients). A significant reduction in serious CMV-associated disease was observed even when patients were stratified according to therapy for transplant rejection (P = 0.04). We observed no effect of immune globulin on rates of viral isolation or seroconversion, suggesting that treated patients often harbored the virus but that clinically evident disease was much less likely to develop in them.

We conclude that CMV immune globulin provides effective prophylaxis in renal-transplant recipients at risk for primary CMV disease. (N Engl J Med 1987; 317: 1049–54.)

Funding and Disclosures

Supported in part by a grant (AM31389) from the National Institutes of Health and a grant (RR-00054) from the General Clinical Research Centers Program of the Division of Research Resources, National Institutes of Health, to New England Medical Center. Some data analysis was performed on the Clinical Study Unit computing facilities of New England Medical Center.

Preliminary results were presented at the Twenty-fifth Interscience Conference on Antimicrobial Agents and Chemotherapy, Minneapolis, September 30 through October 2, 1985, and at the Fifth Annual Meeting of the American Society of Transplant Physicians, Chicago, May 26 through 28, 1986.

We are indebted to Martin S. Hirsch, M.D., Robert H. Rubin, M.D., and Anthony Monaco, M.D., for assistance in case reviews; to Ann Bennett for statistical and organizational assistance; to Mary Elizabeth Mather, Patricia Cedeno, Richard Hovestadt, Katherine Gifford, Michele Pitoniak, Robert Salman, Beverly LaVally, R.N., and many others at the central laboratory; and to Bruce Zalneraitis at the Organ Bank, Jane Goguen at Tissue Typing, Michelle Topor, R.N., Monica Hynes, R.N., Anita Riley, R.N., Patricia Noga, R.N., and all the others at participating centers whose cooperation was invaluable.

Author Affiliations

From the Departments of Medicine, Surgery, and Pediatrics, New England Medical Center, Brigham and Women's Hospital, Children's Hospital, Beth Israel Hospital, and University Hospital, Boston; Boston Veterans Administration Hospital; University Hospital, Denver; New England Organ Bank, Tufts University School of Medicine, Harvard Medical School, and Boston University School of Medicine, Boston; University of Colorado School of Medicine, Denver; and the Massachusetts Public Health Biologic Laboratories, State Laboratory Institute, Massachusetts Department of Public Health, Boston. Address reprint requests to Dr. Snydman at Box 238, New England Medical Center, 750 Washington St., Boston, MA 02111.

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