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Eosinophilia and progression to active tuberculosis in HIV-1-infected Ugandans

Identifieur interne : 004E74 ( Istex/Corpus ); précédent : 004E73; suivant : 004E75

Eosinophilia and progression to active tuberculosis in HIV-1-infected Ugandans

Auteurs : Alison M. Elliott ; Jacqueline Kyosiimire ; Maria A. Quigley ; Jessica Nakiyingi ; Christine Watera ; Michael Brown ; Sarah Joseph ; Neil French ; Charles F. Gilks ; James A. G. Whitworth

Source :

RBID : ISTEX:F1C6284293048E892E0A7AF5995F18D7672E35F8

English descriptors

Abstract

It has been suggested that type 1 immune responses protect against tuberculosis (TB), while type 2 responses, such as those induced by helminths, may suppress protective responses and increase susceptibility to TB. Factors associated with progression to active TB were investigated in a cohort of HIV-1-infected Ugandan adults, a group at high risk of TB. High rates of subsequent progression to active TB were associated with eosinophil counts ⩾ 0.4 × 109/L at enrolment. Eosinophilia at enrolment was associated with male gender, low socio-economic status, high CD4+ T cell counts, and schistosomiasis, but adjusting for these factors did not explain the association of eosinophilia with progression to active TB (adjusted rate ratio = 2.76, P = 0.004). Eosinophilia is most likely to be indicative of a type 2 immune response induced by helminth infection in this Ugandan cohort, but the mechanism of the observed association between eosinophilia and risk of TB remains to be determined.

Url:
DOI: 10.1016/S0035-9203(03)90096-4

Links to Exploration step

ISTEX:F1C6284293048E892E0A7AF5995F18D7672E35F8

Le document en format XML

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<p>It has been suggested that type 1 immune responses protect against tuberculosis (TB), while type 2 responses, such as those induced by helminths, may suppress protective responses and increase susceptibility to TB. Factors associated with progression to active TB were investigated in a cohort of HIV-1-infected Ugandan adults, a group at high risk of TB. High rates of subsequent progression to active TB were associated with eosinophil counts ⩾ 0.4 × 109/L at enrolment. Eosinophilia at enrolment was associated with male gender, low socio-economic status, high CD4+ T cell counts, and schistosomiasis, but adjusting for these factors did not explain the association of eosinophilia with progression to active TB (adjusted rate ratio = 2.76, P = 0.004). Eosinophilia is most likely to be indicative of a type 2 immune response induced by helminth infection in this Ugandan cohort, but the mechanism of the observed association between eosinophilia and risk of TB remains to be determined.</p>
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<term>HIV</term>
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<term>eosinophilia</term>
</item>
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<journal-title>Transactions of The Royal Society of Tropical Medicine and Hygiene</journal-title>
<abbrev-journal-title>Trans R Soc Trop Med Hyg</abbrev-journal-title>
<issn pub-type="ppub">0035-9203</issn>
<issn pub-type="epub">1878-3503</issn>
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<publisher-name>Royal Society of Tropical Medicine and Hygiene</publisher-name>
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<article-id pub-id-type="doi">10.1016/S0035-9203(03)90096-4</article-id>
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<subject>Article</subject>
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<title-group>
<article-title>Eosinophilia and progression to active tuberculosis in HIV-1-infected Ugandans</article-title>
</title-group>
<contrib-group>
<contrib contrib-type="author" corresp="yes">
<name>
<surname>Elliott</surname>
<given-names>Alison M.</given-names>
</name>
<xref ref-type="corresp" rid="COR1">
<sup></sup>
</xref>
<xref ref-type="aff" rid="AFF1">
<sup>1</sup>
</xref>
<xref ref-type="aff" rid="AFF2">
<sup>2</sup>
</xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Kyosiimire</surname>
<given-names>Jacqueline</given-names>
</name>
<xref ref-type="aff" rid="AFF1">
<sup>1</sup>
</xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Quigley</surname>
<given-names>Maria A.</given-names>
</name>
<xref ref-type="aff" rid="AFF2">
<sup>2</sup>
</xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Nakiyingi</surname>
<given-names>Jessica</given-names>
</name>
<xref ref-type="aff" rid="AFF1">
<sup>1</sup>
</xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Watera</surname>
<given-names>Christine</given-names>
</name>
<xref ref-type="aff" rid="AFF1">
<sup>1</sup>
</xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Brown</surname>
<given-names>Michael</given-names>
</name>
<xref ref-type="aff" rid="AFF1">
<sup>1</sup>
</xref>
<xref ref-type="aff" rid="AFF2">
<sup>2</sup>
</xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Joseph</surname>
<given-names>Sarah</given-names>
</name>
<xref ref-type="aff" rid="AFF3">
<sup>3</sup>
</xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>French</surname>
<given-names>Neil</given-names>
</name>
<xref ref-type="aff" rid="AFF4">
<sup>4</sup>
</xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Gilks</surname>
<given-names>Charles F.</given-names>
</name>
<xref ref-type="aff" rid="AFF5">
<sup>5</sup>
</xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Whitworth</surname>
<given-names>James A.G.</given-names>
</name>
<xref ref-type="aff" rid="AFF1">
<sup>1</sup>
</xref>
<xref ref-type="aff" rid="AFF2">
<sup>2</sup>
</xref>
</contrib>
<aff id="AFF1">
<label>1</label>
Uganda Virus Research Institute, P. O. Box 49, Entebbe, Uganda</aff>
<aff id="AFF2">
<label>2</label>
Department of Infectious and Tropical Diseases, London School of Hygiene and Tropical Medicine, Keppel Street, London WC1E 7HT, UK</aff>
<aff id="AFF3">
<label>3</label>
Department of Pathology, University of Cambridge, Tennis Court Road, Cambridge CB2 1QP, UK</aff>
<aff id="AFF4">
<label>4</label>
Liverpool School of Tropical Medicine, Pembroke Place, Liverpool L3 5QA, UK</aff>
<aff id="AFF5">
<label>5</label>
Department of Medicine, Imperial College, St Mary's Campus, Norfolk Place, London W2 1PG, UK</aff>
</contrib-group>
<author-notes>
<corresp id="COR1">
<label></label>
Address for correspondence: Dr A. M. Elliott, Uganda Virus Research Institute, P.O. Box 49, Entebbe, Uganda; phone +256 41 320272, fax +256 41 321173
<email>mrc@starcom.co.ug</email>
</corresp>
</author-notes>
<pub-date pub-type="ppub">
<month>8</month>
<year>2003</year>
</pub-date>
<volume>97</volume>
<issue>4</issue>
<fpage>477</fpage>
<lpage>480</lpage>
<history>
<date date-type="received">
<day>14</day>
<month>10</month>
<year>2002</year>
</date>
<date date-type="rev-recd">
<day>9</day>
<month>1</month>
<year>2003</year>
</date>
<date date-type="accepted">
<day>14</day>
<month>1</month>
<year>2003</year>
</date>
</history>
<permissions>
<copyright-year>2003</copyright-year>
</permissions>
<abstract>
<p>It has been suggested that type 1 immune responses protect against tuberculosis (TB), while type 2 responses, such as those induced by helminths, may suppress protective responses and increase susceptibility to TB. Factors associated with progression to active TB were investigated in a cohort of HIV-1-infected Ugandan adults, a group at high risk of TB. High rates of subsequent progression to active TB were associated with eosinophil counts ⩾ 0.4 × 10
<sup>9</sup>
/L at enrolment. Eosinophilia at enrolment was associated with male gender, low socio-economic status, high CD4+ T cell counts, and schistosomiasis, but adjusting for these factors did not explain the association of eosinophilia with progression to active TB (adjusted rate ratio = 2.76,
<italic>P</italic>
= 0.004). Eosinophilia is most likely to be indicative of a type 2 immune response induced by helminth infection in this Ugandan cohort, but the mechanism of the observed association between eosinophilia and risk of TB remains to be determined.</p>
</abstract>
<kwd-group xml:lang="en">
<title>Keywords</title>
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<kwd>HIV</kwd>
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<kwd>Uganda</kwd>
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<meta-value>July-August 2003</meta-value>
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<back>
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<title>Eosinophilia and progression to active tuberculosis in HIV-1-infected Ugandans</title>
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<title>Eosinophilia and progression to active tuberculosis in HIV-1-infected Ugandans</title>
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<name type="personal" displayLabel="corresp">
<namePart type="given">Alison M.</namePart>
<namePart type="family">Elliott</namePart>
<affiliation>Uganda Virus Research Institute, P. O. Box 49, Entebbe, Uganda</affiliation>
<affiliation>Department of Infectious and Tropical Diseases, London School of Hygiene and Tropical Medicine, Keppel Street, London WC1E 7HT, UK</affiliation>
<affiliation>E-mail: mrc@starcom.co.ug</affiliation>
<affiliation></affiliation>
<affiliation>E-mail: mrc@starcom.co.ug</affiliation>
<role>
<roleTerm type="text">author</roleTerm>
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</name>
<name type="personal">
<namePart type="given">Jacqueline</namePart>
<namePart type="family">Kyosiimire</namePart>
<affiliation>Uganda Virus Research Institute, P. O. Box 49, Entebbe, Uganda</affiliation>
<role>
<roleTerm type="text">author</roleTerm>
</role>
</name>
<name type="personal">
<namePart type="given">Maria A.</namePart>
<namePart type="family">Quigley</namePart>
<affiliation>Department of Infectious and Tropical Diseases, London School of Hygiene and Tropical Medicine, Keppel Street, London WC1E 7HT, UK</affiliation>
<role>
<roleTerm type="text">author</roleTerm>
</role>
</name>
<name type="personal">
<namePart type="given">Jessica</namePart>
<namePart type="family">Nakiyingi</namePart>
<affiliation>Uganda Virus Research Institute, P. O. Box 49, Entebbe, Uganda</affiliation>
<role>
<roleTerm type="text">author</roleTerm>
</role>
</name>
<name type="personal">
<namePart type="given">Christine</namePart>
<namePart type="family">Watera</namePart>
<affiliation>Uganda Virus Research Institute, P. O. Box 49, Entebbe, Uganda</affiliation>
<role>
<roleTerm type="text">author</roleTerm>
</role>
</name>
<name type="personal">
<namePart type="given">Michael</namePart>
<namePart type="family">Brown</namePart>
<affiliation>Uganda Virus Research Institute, P. O. Box 49, Entebbe, Uganda</affiliation>
<affiliation>Department of Infectious and Tropical Diseases, London School of Hygiene and Tropical Medicine, Keppel Street, London WC1E 7HT, UK</affiliation>
<role>
<roleTerm type="text">author</roleTerm>
</role>
</name>
<name type="personal">
<namePart type="given">Sarah</namePart>
<namePart type="family">Joseph</namePart>
<affiliation>Department of Pathology, University of Cambridge, Tennis Court Road, Cambridge CB2 1QP, UK</affiliation>
<role>
<roleTerm type="text">author</roleTerm>
</role>
</name>
<name type="personal">
<namePart type="given">Neil</namePart>
<namePart type="family">French</namePart>
<affiliation>Liverpool School of Tropical Medicine, Pembroke Place, Liverpool L3 5QA, UK</affiliation>
<role>
<roleTerm type="text">author</roleTerm>
</role>
</name>
<name type="personal">
<namePart type="given">Charles F.</namePart>
<namePart type="family">Gilks</namePart>
<affiliation>Department of Medicine, Imperial College, St Mary's Campus, Norfolk Place, London W2 1PG, UK</affiliation>
<role>
<roleTerm type="text">author</roleTerm>
</role>
</name>
<name type="personal">
<namePart type="given">James A.G.</namePart>
<namePart type="family">Whitworth</namePart>
<affiliation>Uganda Virus Research Institute, P. O. Box 49, Entebbe, Uganda</affiliation>
<affiliation>Department of Infectious and Tropical Diseases, London School of Hygiene and Tropical Medicine, Keppel Street, London WC1E 7HT, UK</affiliation>
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<publisher>Royal Society of Tropical Medicine and Hygiene</publisher>
<dateIssued encoding="w3cdtf">2003-08</dateIssued>
<copyrightDate encoding="w3cdtf">2003</copyrightDate>
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<abstract>It has been suggested that type 1 immune responses protect against tuberculosis (TB), while type 2 responses, such as those induced by helminths, may suppress protective responses and increase susceptibility to TB. Factors associated with progression to active TB were investigated in a cohort of HIV-1-infected Ugandan adults, a group at high risk of TB. High rates of subsequent progression to active TB were associated with eosinophil counts ⩾ 0.4 × 109/L at enrolment. Eosinophilia at enrolment was associated with male gender, low socio-economic status, high CD4+ T cell counts, and schistosomiasis, but adjusting for these factors did not explain the association of eosinophilia with progression to active TB (adjusted rate ratio = 2.76, P = 0.004). Eosinophilia is most likely to be indicative of a type 2 immune response induced by helminth infection in this Ugandan cohort, but the mechanism of the observed association between eosinophilia and risk of TB remains to be determined.</abstract>
<subject lang="en">
<genre>Keywords</genre>
<topic>tuberculosis</topic>
<topic>HIV</topic>
<topic>eosinophilia</topic>
<topic>Uganda</topic>
</subject>
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<title>Transactions of The Royal Society of Tropical Medicine and Hygiene</title>
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<title>Trans R Soc Trop Med Hyg</title>
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<identifier type="ISSN">0035-9203</identifier>
<identifier type="eISSN">1878-3503</identifier>
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<part>
<date>2003</date>
<detail type="volume">
<caption>vol.</caption>
<number>97</number>
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<caption>no.</caption>
<number>4</number>
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<end>480</end>
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