Distribution of p24 HTLV3 major core protein in lymph nodes of LAS patients.

Lymph nodes of patients with lymphadenopathy syndrome (LAS) are characterized by two main histological patterns: hyperplastic reactive (H) and regressive (R). In both conditions, the paracortex (PC) is markedly activated with presence of selectively Ia-1+ high endothelial venules. Using a monoclonal...

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Main Authors: Baroni, C, Pezzella, F
Format: Journal article
Language:English
Published: 1987
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author Baroni, C
Pezzella, F
author_facet Baroni, C
Pezzella, F
author_sort Baroni, C
collection OXFORD
description Lymph nodes of patients with lymphadenopathy syndrome (LAS) are characterized by two main histological patterns: hyperplastic reactive (H) and regressive (R). In both conditions, the paracortex (PC) is markedly activated with presence of selectively Ia-1+ high endothelial venules. Using a monoclonal antibody for p24, the major core protein of HTLV3, we have immunohistochemically determined the distribution of p24+ cells in lymph nodes from 23 LAS patients' HTLV3-ab serologically positive. p24+ cells were demonstrated in 11 cases. Control nodes were negative. p24+ cells included high endothelial cells of PC postcapillary venules, large perivenular cells, large mono- or binucleated cells in PC and in GC, and few lymphocytelike cells. Our preliminary observations indicate that the majority of p24+ cells are high endothelial and accessory cells that may act either as virus reservoir or as antigen-presenting cells to T4 lymphocytes and to GC B cells. In addition, the positivity of high endothelial cells for p24 might help to explain their selective Ia-1+.
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spelling oxford-uuid:17e5a2e7-f0d6-45bf-b03f-a2fed2c0363c2022-03-26T10:40:12ZDistribution of p24 HTLV3 major core protein in lymph nodes of LAS patients.Journal articlehttp://purl.org/coar/resource_type/c_dcae04bcuuid:17e5a2e7-f0d6-45bf-b03f-a2fed2c0363cEnglishSymplectic Elements at Oxford1987Baroni, CPezzella, FLymph nodes of patients with lymphadenopathy syndrome (LAS) are characterized by two main histological patterns: hyperplastic reactive (H) and regressive (R). In both conditions, the paracortex (PC) is markedly activated with presence of selectively Ia-1+ high endothelial venules. Using a monoclonal antibody for p24, the major core protein of HTLV3, we have immunohistochemically determined the distribution of p24+ cells in lymph nodes from 23 LAS patients' HTLV3-ab serologically positive. p24+ cells were demonstrated in 11 cases. Control nodes were negative. p24+ cells included high endothelial cells of PC postcapillary venules, large perivenular cells, large mono- or binucleated cells in PC and in GC, and few lymphocytelike cells. Our preliminary observations indicate that the majority of p24+ cells are high endothelial and accessory cells that may act either as virus reservoir or as antigen-presenting cells to T4 lymphocytes and to GC B cells. In addition, the positivity of high endothelial cells for p24 might help to explain their selective Ia-1+.
spellingShingle Baroni, C
Pezzella, F
Distribution of p24 HTLV3 major core protein in lymph nodes of LAS patients.
title Distribution of p24 HTLV3 major core protein in lymph nodes of LAS patients.
title_full Distribution of p24 HTLV3 major core protein in lymph nodes of LAS patients.
title_fullStr Distribution of p24 HTLV3 major core protein in lymph nodes of LAS patients.
title_full_unstemmed Distribution of p24 HTLV3 major core protein in lymph nodes of LAS patients.
title_short Distribution of p24 HTLV3 major core protein in lymph nodes of LAS patients.
title_sort distribution of p24 htlv3 major core protein in lymph nodes of las patients
work_keys_str_mv AT baronic distributionofp24htlv3majorcoreproteininlymphnodesoflaspatients
AT pezzellaf distributionofp24htlv3majorcoreproteininlymphnodesoflaspatients