Serveur d'exploration sur le lymphœdème

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Evidence for Protective Immunity to Bancroftian Filariasis in the Cook Islands

Identifieur interne : 00BE69 ( Main/Exploration ); précédent : 00BE68; suivant : 00BE70

Evidence for Protective Immunity to Bancroftian Filariasis in the Cook Islands

Auteurs : Cathy Steel [Îles Cook] ; Archibald Guinea [Îles Cook] ; Eric A. Ottesen [Îles Cook]

Source :

RBID : ISTEX:FB6C073CED0119FB63A58E469E12F6DAC1538D05

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English descriptors

Abstract

To challenge the concept of protective immunity in lymphatic filariasis, 19 adult residents of a Wuchereria bancrofti-endemic island who had been diagnosed 17 years earlier as putatively immune endemic normals (PI/EN) were reexamined. Even with continued exposure to infection, all 19 had maintained their apparent infection-free status. Studies to define the mechanisms underlying this putative immunity revealed that cellular immune responses (including proliferation; generation of interleukin [IL]-2, IL-5, IL-10, interferon-y, and granulocyte-macrophage colony-stimulating factor) to adult- and microfilarial-stage antigens, but not antibody responses, were markedly greater than those of 20 age-matched, infected patients. Furthermore, the PI/EN group was comprised of highand low-responding persons who were clinically indistinguishable. These findings provide evidence that protective immunity to lymphatic filariasis does occur and that it is probably T cell-mediated.

Url:
DOI: 10.1093/infdis/174.3.598


Affiliations:


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Le document en format XML

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<div type="abstract">To challenge the concept of protective immunity in lymphatic filariasis, 19 adult residents of a Wuchereria bancrofti-endemic island who had been diagnosed 17 years earlier as putatively immune endemic normals (PI/EN) were reexamined. Even with continued exposure to infection, all 19 had maintained their apparent infection-free status. Studies to define the mechanisms underlying this putative immunity revealed that cellular immune responses (including proliferation; generation of interleukin [IL]-2, IL-5, IL-10, interferon-y, and granulocyte-macrophage colony-stimulating factor) to adult- and microfilarial-stage antigens, but not antibody responses, were markedly greater than those of 20 age-matched, infected patients. Furthermore, the PI/EN group was comprised of highand low-responding persons who were clinically indistinguishable. These findings provide evidence that protective immunity to lymphatic filariasis does occur and that it is probably T cell-mediated.</div>
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