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PMID: 6088649 Published · ppublish English Journal Article Research Support, U.S. Gov't, P.H.S.

Defective polymorphonuclear leukocyte chemotaxis in homosexual men with persistent lymph node syndrome.

The Journal of infectious diseases ·Vol. 150 ·No. 2 ·1984-08-00 ·Pages 267-71

Valone FH, Payan DG, Abrams DI, Goetzl EJ

Abstract

Persistent lymph node syndrome, epidemiologically related to acquired immune deficiency syndrome, is characterized by reactive lymphadenopathy and an increased incidence of localized bacterial, viral, and fungal infections. Seven typical patients were found to have a localized infection every 4.5 +/- 2.0 months (mean +/- SD) since onset of adenopathy. Because recurrent bacterial infections may be associated with defective polymorphonuclear leukocyte (PMNL) function, studies of PMNL function in these patients were undertaken. The patients' PMNLs had diminished chemotactic responses to high concentrations of two structurally distinct chemotactic factors, leukotriene B4 and N-formylmethionylleucylphenylalanine. The patients' PMNLs also had deficient degranulating responses to the former but not to the latter. Diminished PMNL function may contribute to the observed increased incidence of localized infections, which are a major source of morbidity, in these patients.

MeSH Terms
Adult Chemotaxis, Leukocyte Glucuronidase/metabolism Homosexuality Humans Leukotriene B4/pharmacology Lymphatic Diseases/blood Lysosomes/enzymology Male N-Formylmethionine Leucyl-Phenylalanine/pharmacology Neutrophils/physiology,ultrastructure Syndrome
Chemicals
Leukotriene B4 N-Formylmethionine Leucyl-Phenylalanine Glucuronidase
Authors & Affiliations
4 authors, click to expand affiliations / ORCID
Valone F H
Payan D G
Abrams D I
Goetzl E J
Article Info
Journal
The Journal of infectious diseases
Abbr.
J Infect Dis
ISSN
0022-1899
Published
1984-08-00
Pages
267-71
Language
English
Region
United States
NLM ID
0413675
Subset
IM
Grants
NIAID NIH HHS · AI-18262 · United States
NIAID NIH HHS · AI-19784 · United States
NHLBI NIH HHS · HL-31809 · United States
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