[Acquired immunodeficiency syndrome with chronic granulomatous inflammation. Clinically definable special form of the variable immunodeficiency syndrome] NLM AIDSLINE Important note: Information in this article was accurate in 1986. The state of the art may have changed since the publication date.

Click here to return to AIDSLINE main menu
DonateNow
Print this Article


[Acquired immunodeficiency syndrome with chronic granulomatous inflammation. Clinically definable special form of the variable immunodeficiency syndrome]

Dtsch Med Wochenschr. 1986 Jan 17;111(3):93-8. Unique Identifier : AIDSLINE MED/86081292
Stoll M; Peter HH; Lange ML; Wolff-Vorbeck G; Kemnitz J; Deicher H


Abstract: Five cases (3 men, 2 women) of late-onset variable immunodeficiency syndrome (CVID), characterized by similar clinical and immunological findings as well as histological demonstration of chronic granulomatous infection, are reported. All patients had frequent attacks of respiratory infections with recurrent bronchitis and pneumonia. In addition to predominating basally localized streaky-nodular lung changes all patients had hepatosplenomegaly and granulomatous infections of other organs. Immunologically, marked hypogammaglobulinaemia of all Ig classes, lymphopenia, and absence of terminal B-cell maturation were predominant. In-vitro tests under pokeweed-mitogen failed to demonstrate terminal plasma-cell differentiation of B-lymphocytes and thus Ig synthesis. Without pokeweed-mitogen there were largely nonsecretory B-blasts with abnormal granulated cytoplasmic Ig formation. Skin testing with Multitest application revealed almost complete anergy, both in the Arthus (24 h) and the late reactions (48 and 72 h). Nonetheless, T-cell reaction in-vitro was much less affected than B-cell function. Natural killing and antibody-dependent cytotoxicity were normal or slightly increased.
Keywords: Acquired Immunodeficiency Syndrome/*IMMUNOLOGY/PATHOLOGY Adolescence Adult Antibody-Dependent Cell Cytotoxicity B-Lymphocytes/IMMUNOLOGY Bone Marrow/PATHOLOGY English Abstract Female Granulomatous Disease, Chronic/*IMMUNOLOGY/PATHOLOGY Human Intradermal Tests Killer Cells, Natural/IMMUNOLOGY Lung/PATHOLOGY Lymphocyte Transformation Male Rosette Formation Support, Non-U.S. Gov't JOURNAL ARTICLE

KWDacquiredimmunodeficiencysyndrome/KWDimmunology/pathologyadolescenceadultantibody-dependentcellcytotoxicityb-lymphocytes/immunologybonemarrow/pathologyenglishabstractfemalegranulomatousdisease,chronic/KWDimmunology/pathologyhumanintradermaltestskillercells,natural/immunologylung/pathologylymphocytetransformationmalerosetteformationsupport,non-uKWDsKWDgov'tjournalarticle
860430
M8640115


Copyright © 1986 - National Library of Medicine. Reproduced under license with the National Library of Medicine, Bethesda, MD.

AEGiS is a 501(c)3, not-for-profit, tax-exempt, educational corporation. AEGiS is made possible through unrestricted funding from Boehringer Ingelheim, Bridgestone/Firestone Charitable Trust, Bristol-Myers Squibb Company, Elton John AIDS Foundation, Gill Foundation, the National Library of Medicine, Quest Diagnostics, Roche and Trimeris, and donations from users like you. Always watch for outdated information. This article first appeared in 1986. This material is designed to support, not replace, the relationship that exists between you and your doctor.

AEGiS presents published material, reprinted with permission and neither endorses nor opposes any material. All information contained on this website, including information relating to health conditions, products, and treatments, is for informational purposes only. It is often presented in summary or aggregate form. It is not meant to be a substitute for the advice provided by your own physician or other medical professionals. Always discuss treatment options with a doctor who specializes in treating HIV.

Copyright ©1980, 1986. AEGiS. All materials appearing on AEGiS are protected by copyright as a collective work or compilation under U.S. copyright and other laws and are the property of AEGiS, or the party credited as the provider of the content. .