Delayed–type hypersensitivity skin testing in human immunodeficiency virus–infected pediatric patients

OBJECTIVE: To evaluate whether pediatric patients infected with human immunodeficiency virus (HIV) can mount appropriate delayed–type hypersensitivity (DTH) skin responses to recall antigens and whether these responses can be correlated with clinical or immunologic parameters. DESIGN: Prospective ev...

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Veröffentlicht in:The Journal of pediatrics 1996-08, Vol.129 (2), p.245-250
Hauptverfasser: Raszka, William V., Moriarty, Richard A., Ottolini, Martin G., Waecker, Norman J., Ascher, David P., Cieslak, Theodore J., Fischer, Gerald W., Robb, Merlin L.
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container_end_page 250
container_issue 2
container_start_page 245
container_title The Journal of pediatrics
container_volume 129
creator Raszka, William V.
Moriarty, Richard A.
Ottolini, Martin G.
Waecker, Norman J.
Ascher, David P.
Cieslak, Theodore J.
Fischer, Gerald W.
Robb, Merlin L.
description OBJECTIVE: To evaluate whether pediatric patients infected with human immunodeficiency virus (HIV) can mount appropriate delayed–type hypersensitivity (DTH) skin responses to recall antigens and whether these responses can be correlated with clinical or immunologic parameters. DESIGN: Prospective evaluation of DTH responses in HIV-infected children. Uninfected children born to HIV-infected mothers served as control subjects. Antigens used for yearly DTH testing included Candida albicans (1:100, 1:10); mumps virus; Trichophyton; purified protein derivative of tuberculin; and tetanus toxoid (1:100, 1:10). At the time of each DTH test, patients were staged according to two Centers for Disease Control and Prevention pediatric HIV classification systems, and T-cell subsets were obtained. RESULTS: Twenty-seven HIV-infected patients with a median age at entry of 74.1 (range, 12 to 156) months were followed. Forty-four DTH skin tests in 21 symptom-free HIV-infected patients (P1) and 18 tests in 10 HIV-infected patients with symptoms (P2), as well as 43 DTH skin tests in 18 patients who had either mild or moderate clinical symptoms or immunosuppression and 19 tests in 13 patients with severe symptoms or immunosuppression, were evaluated. Sixteen DTH skin tests were performed in 14 uninfected patients. HIV-infected patients tended to have fewer DTH responses to antigens and of smaller size than did uninfected patients. When controlled for age, few differences in DTH responsiveness were seen between HIV-infected and uninfected patients. Anergy was associated with symptomatic disease, evidence of advanced clinical or immunologic disease, and low CD4 + percentages ( p
doi_str_mv 10.1016/S0022-3476(96)70249-4
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DESIGN: Prospective evaluation of DTH responses in HIV-infected children. Uninfected children born to HIV-infected mothers served as control subjects. Antigens used for yearly DTH testing included Candida albicans (1:100, 1:10); mumps virus; Trichophyton; purified protein derivative of tuberculin; and tetanus toxoid (1:100, 1:10). At the time of each DTH test, patients were staged according to two Centers for Disease Control and Prevention pediatric HIV classification systems, and T-cell subsets were obtained. RESULTS: Twenty-seven HIV-infected patients with a median age at entry of 74.1 (range, 12 to 156) months were followed. Forty-four DTH skin tests in 21 symptom-free HIV-infected patients (P1) and 18 tests in 10 HIV-infected patients with symptoms (P2), as well as 43 DTH skin tests in 18 patients who had either mild or moderate clinical symptoms or immunosuppression and 19 tests in 13 patients with severe symptoms or immunosuppression, were evaluated. Sixteen DTH skin tests were performed in 14 uninfected patients. HIV-infected patients tended to have fewer DTH responses to antigens and of smaller size than did uninfected patients. When controlled for age, few differences in DTH responsiveness were seen between HIV-infected and uninfected patients. Anergy was associated with symptomatic disease, evidence of advanced clinical or immunologic disease, and low CD4 + percentages ( p &lt;0.05). CONCLUSIONS: HIV-infected children are able to mount antigen-specific cell-mediated immune responses that are qualitatively similar to those of age-matched control subjects. Loss of DTH responsiveness correlates with both clinical and immunologic evidence of HIV disease progression. (J P EDIATR 1996;129:245-50)</description><identifier>ISSN: 0022-3476</identifier><identifier>EISSN: 1097-6833</identifier><identifier>DOI: 10.1016/S0022-3476(96)70249-4</identifier><identifier>PMID: 8765622</identifier><identifier>CODEN: JOPDAB</identifier><language>eng</language><publisher>New York, NY: Mosby, Inc</publisher><subject>Adolescent ; Age Factors ; AIDS/HIV ; Antigens - immunology ; Antigens, Fungal - immunology ; Antigens, Viral - immunology ; Biological and medical sciences ; Candida albicans - immunology ; Case-Control Studies ; CD4 Lymphocyte Count ; Child ; Child, Preschool ; Follow-Up Studies ; HIV Infections - immunology ; Humans ; Hypersensitivity, Delayed - immunology ; Immunocompromised Host ; Immunodeficiencies ; Immunodeficiencies. Immunoglobulinopathies ; Immunologic Memory ; Immunopathology ; Infant ; Lymphocyte Count ; Medical sciences ; Mumps virus - immunology ; Prospective Studies ; Skin - immunology ; Skin Tests ; T-Lymphocyte Subsets - pathology ; Tetanus Toxoid ; Trichophyton - immunology ; Tuberculin</subject><ispartof>The Journal of pediatrics, 1996-08, Vol.129 (2), p.245-250</ispartof><rights>1996</rights><rights>1996 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c389t-46d2071106028ebc9ea762f3339b638a6dd41d129de44dac8fb49734211a35463</citedby><cites>FETCH-LOGICAL-c389t-46d2071106028ebc9ea762f3339b638a6dd41d129de44dac8fb49734211a35463</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S0022347696702494$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,776,780,3537,27901,27902,65306</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&amp;idt=3182295$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/8765622$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Raszka, William V.</creatorcontrib><creatorcontrib>Moriarty, Richard A.</creatorcontrib><creatorcontrib>Ottolini, Martin G.</creatorcontrib><creatorcontrib>Waecker, Norman J.</creatorcontrib><creatorcontrib>Ascher, David P.</creatorcontrib><creatorcontrib>Cieslak, Theodore J.</creatorcontrib><creatorcontrib>Fischer, Gerald W.</creatorcontrib><creatorcontrib>Robb, Merlin L.</creatorcontrib><creatorcontrib>9/21/74361</creatorcontrib><creatorcontrib>The views expressed in this article are those of the authors and do not reflect the official policy or position of the Department of the Army, the Department of Defense, or the United States Government</creatorcontrib><title>Delayed–type hypersensitivity skin testing in human immunodeficiency virus–infected pediatric patients</title><title>The Journal of pediatrics</title><addtitle>J Pediatr</addtitle><description>OBJECTIVE: To evaluate whether pediatric patients infected with human immunodeficiency virus (HIV) can mount appropriate delayed–type hypersensitivity (DTH) skin responses to recall antigens and whether these responses can be correlated with clinical or immunologic parameters. DESIGN: Prospective evaluation of DTH responses in HIV-infected children. Uninfected children born to HIV-infected mothers served as control subjects. Antigens used for yearly DTH testing included Candida albicans (1:100, 1:10); mumps virus; Trichophyton; purified protein derivative of tuberculin; and tetanus toxoid (1:100, 1:10). At the time of each DTH test, patients were staged according to two Centers for Disease Control and Prevention pediatric HIV classification systems, and T-cell subsets were obtained. RESULTS: Twenty-seven HIV-infected patients with a median age at entry of 74.1 (range, 12 to 156) months were followed. Forty-four DTH skin tests in 21 symptom-free HIV-infected patients (P1) and 18 tests in 10 HIV-infected patients with symptoms (P2), as well as 43 DTH skin tests in 18 patients who had either mild or moderate clinical symptoms or immunosuppression and 19 tests in 13 patients with severe symptoms or immunosuppression, were evaluated. Sixteen DTH skin tests were performed in 14 uninfected patients. HIV-infected patients tended to have fewer DTH responses to antigens and of smaller size than did uninfected patients. When controlled for age, few differences in DTH responsiveness were seen between HIV-infected and uninfected patients. Anergy was associated with symptomatic disease, evidence of advanced clinical or immunologic disease, and low CD4 + percentages ( p &lt;0.05). CONCLUSIONS: HIV-infected children are able to mount antigen-specific cell-mediated immune responses that are qualitatively similar to those of age-matched control subjects. Loss of DTH responsiveness correlates with both clinical and immunologic evidence of HIV disease progression. (J P EDIATR 1996;129:245-50)</description><subject>Adolescent</subject><subject>Age Factors</subject><subject>AIDS/HIV</subject><subject>Antigens - immunology</subject><subject>Antigens, Fungal - immunology</subject><subject>Antigens, Viral - immunology</subject><subject>Biological and medical sciences</subject><subject>Candida albicans - immunology</subject><subject>Case-Control Studies</subject><subject>CD4 Lymphocyte Count</subject><subject>Child</subject><subject>Child, Preschool</subject><subject>Follow-Up Studies</subject><subject>HIV Infections - immunology</subject><subject>Humans</subject><subject>Hypersensitivity, Delayed - immunology</subject><subject>Immunocompromised Host</subject><subject>Immunodeficiencies</subject><subject>Immunodeficiencies. Immunoglobulinopathies</subject><subject>Immunologic Memory</subject><subject>Immunopathology</subject><subject>Infant</subject><subject>Lymphocyte Count</subject><subject>Medical sciences</subject><subject>Mumps virus - immunology</subject><subject>Prospective Studies</subject><subject>Skin - immunology</subject><subject>Skin Tests</subject><subject>T-Lymphocyte Subsets - pathology</subject><subject>Tetanus Toxoid</subject><subject>Trichophyton - immunology</subject><subject>Tuberculin</subject><issn>0022-3476</issn><issn>1097-6833</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1996</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkM1O3DAQgC1ERRfKIyDlgBA9pPhv7fhUIShtJSQObc-W154UQ-KktrNSbn2HviFPgtld7bWXmZHmmx99CJ0R_IlgIq5-YExpzbgUl0p8lJhyVfMDtCBYyVo0jB2ixR55j45TesIYK47xETpqpFgKShfo6RY6M4N7-fsvzyNUjyXEBCH57Nc-z1V69qHKkLIPv6tSPk69CZXv-ykMDlpvPQQ7V2sfp1SW-NCCzeCqEZw3OXpbjSYXJqcP6F1rugSnu3yCft19-Xnzrb5_-Pr95vq-tqxRuebCUSwJwQLTBlZWgZGCtowxtRKsMcI5ThyhygHnztimXXElGaeEGLbkgp2gi-3eMQ5_pvK57n2y0HUmwDAlLZuiSipWwOUWtHFIKUKrx-h7E2dNsH5zrDeO9ZtArYTeONa8zJ3tDkyrHtx-aie19M93fZOs6dpogvVpjzHSUKqWBfu8xaDIWHuIOm1kFnGxONRu8P955BXHbZxZ</recordid><startdate>19960801</startdate><enddate>19960801</enddate><creator>Raszka, William V.</creator><creator>Moriarty, Richard A.</creator><creator>Ottolini, Martin G.</creator><creator>Waecker, Norman J.</creator><creator>Ascher, David P.</creator><creator>Cieslak, Theodore J.</creator><creator>Fischer, Gerald W.</creator><creator>Robb, Merlin L.</creator><general>Mosby, Inc</general><general>Elsevier</general><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>19960801</creationdate><title>Delayed–type hypersensitivity skin testing in human immunodeficiency virus–infected pediatric patients</title><author>Raszka, William V. ; Moriarty, Richard A. ; Ottolini, Martin G. ; Waecker, Norman J. ; Ascher, David P. ; Cieslak, Theodore J. ; Fischer, Gerald W. ; Robb, Merlin L.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c389t-46d2071106028ebc9ea762f3339b638a6dd41d129de44dac8fb49734211a35463</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1996</creationdate><topic>Adolescent</topic><topic>Age Factors</topic><topic>AIDS/HIV</topic><topic>Antigens - immunology</topic><topic>Antigens, Fungal - immunology</topic><topic>Antigens, Viral - immunology</topic><topic>Biological and medical sciences</topic><topic>Candida albicans - immunology</topic><topic>Case-Control Studies</topic><topic>CD4 Lymphocyte Count</topic><topic>Child</topic><topic>Child, Preschool</topic><topic>Follow-Up Studies</topic><topic>HIV Infections - immunology</topic><topic>Humans</topic><topic>Hypersensitivity, Delayed - immunology</topic><topic>Immunocompromised Host</topic><topic>Immunodeficiencies</topic><topic>Immunodeficiencies. Immunoglobulinopathies</topic><topic>Immunologic Memory</topic><topic>Immunopathology</topic><topic>Infant</topic><topic>Lymphocyte Count</topic><topic>Medical sciences</topic><topic>Mumps virus - immunology</topic><topic>Prospective Studies</topic><topic>Skin - immunology</topic><topic>Skin Tests</topic><topic>T-Lymphocyte Subsets - pathology</topic><topic>Tetanus Toxoid</topic><topic>Trichophyton - immunology</topic><topic>Tuberculin</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Raszka, William V.</creatorcontrib><creatorcontrib>Moriarty, Richard A.</creatorcontrib><creatorcontrib>Ottolini, Martin G.</creatorcontrib><creatorcontrib>Waecker, Norman J.</creatorcontrib><creatorcontrib>Ascher, David P.</creatorcontrib><creatorcontrib>Cieslak, Theodore J.</creatorcontrib><creatorcontrib>Fischer, Gerald W.</creatorcontrib><creatorcontrib>Robb, Merlin L.</creatorcontrib><creatorcontrib>9/21/74361</creatorcontrib><creatorcontrib>The views expressed in this article are those of the authors and do not reflect the official policy or position of the Department of the Army, the Department of Defense, or the United States Government</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>The Journal of pediatrics</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Raszka, William V.</au><au>Moriarty, Richard A.</au><au>Ottolini, Martin G.</au><au>Waecker, Norman J.</au><au>Ascher, David P.</au><au>Cieslak, Theodore J.</au><au>Fischer, Gerald W.</au><au>Robb, Merlin L.</au><aucorp>9/21/74361</aucorp><aucorp>The views expressed in this article are those of the authors and do not reflect the official policy or position of the Department of the Army, the Department of Defense, or the United States Government</aucorp><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Delayed–type hypersensitivity skin testing in human immunodeficiency virus–infected pediatric patients</atitle><jtitle>The Journal of pediatrics</jtitle><addtitle>J Pediatr</addtitle><date>1996-08-01</date><risdate>1996</risdate><volume>129</volume><issue>2</issue><spage>245</spage><epage>250</epage><pages>245-250</pages><issn>0022-3476</issn><eissn>1097-6833</eissn><coden>JOPDAB</coden><abstract>OBJECTIVE: To evaluate whether pediatric patients infected with human immunodeficiency virus (HIV) can mount appropriate delayed–type hypersensitivity (DTH) skin responses to recall antigens and whether these responses can be correlated with clinical or immunologic parameters. DESIGN: Prospective evaluation of DTH responses in HIV-infected children. Uninfected children born to HIV-infected mothers served as control subjects. Antigens used for yearly DTH testing included Candida albicans (1:100, 1:10); mumps virus; Trichophyton; purified protein derivative of tuberculin; and tetanus toxoid (1:100, 1:10). At the time of each DTH test, patients were staged according to two Centers for Disease Control and Prevention pediatric HIV classification systems, and T-cell subsets were obtained. RESULTS: Twenty-seven HIV-infected patients with a median age at entry of 74.1 (range, 12 to 156) months were followed. Forty-four DTH skin tests in 21 symptom-free HIV-infected patients (P1) and 18 tests in 10 HIV-infected patients with symptoms (P2), as well as 43 DTH skin tests in 18 patients who had either mild or moderate clinical symptoms or immunosuppression and 19 tests in 13 patients with severe symptoms or immunosuppression, were evaluated. Sixteen DTH skin tests were performed in 14 uninfected patients. HIV-infected patients tended to have fewer DTH responses to antigens and of smaller size than did uninfected patients. When controlled for age, few differences in DTH responsiveness were seen between HIV-infected and uninfected patients. Anergy was associated with symptomatic disease, evidence of advanced clinical or immunologic disease, and low CD4 + percentages ( p &lt;0.05). CONCLUSIONS: HIV-infected children are able to mount antigen-specific cell-mediated immune responses that are qualitatively similar to those of age-matched control subjects. Loss of DTH responsiveness correlates with both clinical and immunologic evidence of HIV disease progression. (J P EDIATR 1996;129:245-50)</abstract><cop>New York, NY</cop><pub>Mosby, Inc</pub><pmid>8765622</pmid><doi>10.1016/S0022-3476(96)70249-4</doi><tpages>6</tpages></addata></record>
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subjects Adolescent
Age Factors
AIDS/HIV
Antigens - immunology
Antigens, Fungal - immunology
Antigens, Viral - immunology
Biological and medical sciences
Candida albicans - immunology
Case-Control Studies
CD4 Lymphocyte Count
Child
Child, Preschool
Follow-Up Studies
HIV Infections - immunology
Humans
Hypersensitivity, Delayed - immunology
Immunocompromised Host
Immunodeficiencies
Immunodeficiencies. Immunoglobulinopathies
Immunologic Memory
Immunopathology
Infant
Lymphocyte Count
Medical sciences
Mumps virus - immunology
Prospective Studies
Skin - immunology
Skin Tests
T-Lymphocyte Subsets - pathology
Tetanus Toxoid
Trichophyton - immunology
Tuberculin
title Delayed–type hypersensitivity skin testing in human immunodeficiency virus–infected pediatric patients
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