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Age, thymopoiesis, and CD4+ T-lymphocyte regeneration after intensive chemotherapy

Authors :
Mackall, Crystal L.
Fleisher, Thomas A.
Brown, Margaret R.
Andrich, Mary P.
Chen, Clara C.
Feuerstein, Irwin M.
Horowitz, Marc E.
Magrath, Ian T.
Shad, Aziza T.
Steinberg, Seth M.
Wexler, Leonard H.
Gress, Ronald E.
Source :
The New England Journal of Medicine. Jan 19, 1995, Vol. v332 Issue n3, p143, 7 p.
Publication Year :
1995

Abstract

Rapid regeneration of immunity following chemotherapy may depend on the function of the thymus, an organ located in the upper chest that produces T lymphocytes. The thymus develops and functions throughout childhood, losing its function gradually after puberty. A study of 15 patients aged 1 to 24 years who had had extensive chemotherapy found an inverse relation between age and CD4+ T lymphocyte counts. The ability of the patients' bodies to regenerate CD4+ T lymphocytes after chemotherapy seemed to diminish with age. T lymphocytes are critical to healthy functioning of the body's immune system. The findings of this study suggest that any disease or therapy that decreases CD4+ T cells may affect adults more than children, as children may regenerate their T cell counts faster because of their functioning thymus. Study results may be applicable to treatments being developed for HIV-positive patients and for persons receiving bone marrow transplants to increase their immune responses.

Details

ISSN :
00284793
Volume :
v332
Issue :
n3
Database :
Gale General OneFile
Journal :
The New England Journal of Medicine
Publication Type :
Academic Journal
Accession number :
edsgcl.16425883