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T cell responsiveness correlates differentially with antibody isotype levels in clinical and asymptomatic filariasis.

Identifieur interne : 00CC11 ( Main/Exploration ); précédent : 00CC10; suivant : 00CC12

T cell responsiveness correlates differentially with antibody isotype levels in clinical and asymptomatic filariasis.

Auteurs : M. Yazdanbakhsh [Pays-Bas] ; W A Paxton ; Y C Kruize ; E. Sartono ; A. Kurniawan ; A. Van Het Wout ; M E Selkirk ; F. Partono ; R M Maizels

Source :

RBID : pubmed:8450257

Descripteurs français

English descriptors

Abstract

To establish the relationships among T and B cell responses, active infection, and clinical manifestations in lymphatic filariasis, filarial-specific lymphocyte proliferation, IgG antibody isotypes, and IgE levels were determined in an exposed population: 31 asymptomatic amicrofilaremics, 43 microfilaremics, 12 symptomatic amicrofilaremics, and 52 elephantiasis patients. Lymphocyte proliferation was higher in elephantiasis patients and asymptomatic amicrofilaremics than in microfilaremics (P < .004). A proportion of asymptomatic amicrofilaremics (32%), elephantiasis patients (37%), and symptomatic amicrofilaremics (58%) showed antigen-specific lymphocyte unresponsiveness, and lymphocyte proliferation to filarial antigens correlated negatively with specific IgG4 levels (rho = -0.315, P < .001). As elevated specific IgG4 is an indicator of active infection, it is argued that active infection may result in lymphocyte hyporesponsiveness irrespective of clinical category. Of those with elevated specific IgE levels and high T cell proliferative responses, 70% had elephantiasis, suggesting these factors have a role in pathology. However, the existence of a proportion of elephantiasis patients with low anti-filarial IgE and T cell unresponsiveness to filarial antigens suggests that elephantiasis can be caused by distinct processes.

PubMed: 8450257


Affiliations:


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Le document en format XML

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<nlm:affiliation>Department of Parasitology, Leiden University, Netherlands.</nlm:affiliation>
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<term>Antibodies, Helminth (analysis)</term>
<term>Antigens, Helminth (administration & dosage)</term>
<term>Antigens, Helminth (immunology)</term>
<term>Elephantiasis, Filarial (immunology)</term>
<term>Eosinophilia (pathology)</term>
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<term>Immunity, Cellular</term>
<term>Immunoglobulin E (analysis)</term>
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<term>Lymphocyte Activation (physiology)</term>
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<term>Activation des lymphocytes (physiologie)</term>
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<term>Adulte d'âge moyen</term>
<term>Anticorps antihelminthe (analyse)</term>
<term>Antigènes d'helminthe (administration et posologie)</term>
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<term>Facteurs de l'âge</term>
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<term>Lymphocytes T (immunologie)</term>
<term>Lymphocytes T (physiologie)</term>
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<div type="abstract" xml:lang="en">To establish the relationships among T and B cell responses, active infection, and clinical manifestations in lymphatic filariasis, filarial-specific lymphocyte proliferation, IgG antibody isotypes, and IgE levels were determined in an exposed population: 31 asymptomatic amicrofilaremics, 43 microfilaremics, 12 symptomatic amicrofilaremics, and 52 elephantiasis patients. Lymphocyte proliferation was higher in elephantiasis patients and asymptomatic amicrofilaremics than in microfilaremics (P < .004). A proportion of asymptomatic amicrofilaremics (32%), elephantiasis patients (37%), and symptomatic amicrofilaremics (58%) showed antigen-specific lymphocyte unresponsiveness, and lymphocyte proliferation to filarial antigens correlated negatively with specific IgG4 levels (rho = -0.315, P < .001). As elevated specific IgG4 is an indicator of active infection, it is argued that active infection may result in lymphocyte hyporesponsiveness irrespective of clinical category. Of those with elevated specific IgE levels and high T cell proliferative responses, 70% had elephantiasis, suggesting these factors have a role in pathology. However, the existence of a proportion of elephantiasis patients with low anti-filarial IgE and T cell unresponsiveness to filarial antigens suggests that elephantiasis can be caused by distinct processes.</div>
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