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PMID: 6318629 Published · ppublish English Journal Article Review

NIH conference. Acquired immunodeficiency syndrome: epidemiologic, clinical, immunologic, and therapeutic considerations.

Annals of internal medicine ·Vol. 100 ·No. 1 ·1984-01-00 ·Pages 92-106

Fauci AS, Macher AM, Longo DL, Lane HC, Rook AH, Masur H, Gelmann EP

Abstract

The acquired immunodeficiency syndrome is a new disease whose cause is unknown but is almost surely due to a transmissible agent, most likely a virus. The disease is clearly spread by sexual contact, particularly homosexual activity. Blood-borne transmission constitutes the other major recognized form of spread of the disease, although it is highly likely that the disease is not readily spread through casual, nonsexual, non-blood-borne routes. Although the disease is still highly concentrated in the United States, it is now seen in several countries throughout the world. The common denominator of the disease is a profound suppression of cell-mediated immunity, specifically a quantitative and qualitative defect in the T4 inducer or helper subset of T lymphocytes. Hyperactivity of B lymphocytes is also characteristic. The clinical manifestations are those of severe and life-threatening opportunistic infections and unusual neoplasms, particularly Kaposi's sarcoma. The mortality may well approach 100%, making this one of the most extraordinary transmissible diseases in history.

MeSH Terms
Acquired Immunodeficiency Syndrome/complications,epidemiology,immunology,therapy Adult Female Humans Infant Infections/etiology Lymphatic Diseases/etiology Male Middle Aged Neoplasms/etiology Retroviridae Infections/immunology Risk Sarcoma, Kaposi/etiology Virus Diseases/immunology
Authors & Affiliations
7 authors, click to expand affiliations / ORCID
Fauci A S
Macher A M
Longo D L
Lane H C
Rook A H
Masur H
Gelmann E P
Article Info
Journal
Annals of internal medicine
Abbr.
Ann Intern Med
ISSN
0003-4819
Published
1984-01-00
Pages
92-106
Language
English
Region
United States
NLM ID
0372351
Subset
IM
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