Comparison of Cross-Reactivities of Imipenem and Other Beta-Lactam Antibiotics by Delayed-Type Hypersensitivity Reaction in Guinea Pigs

The cross-reactivity of imipenem (IPM) in a delayed-type hypersensitivity (DTH) reaction was investigated by intradermal skin reaction, macrophage migration inhibition tests (MIT) and lymphocyte stimulation tests (LST) in guinea pigs. The animals were immunized with IPM, ampicillin (ABPC) or cephale...

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Veröffentlicht in:Chemical & pharmaceutical bulletin 1991/03/25, Vol.39(3), pp.765-768
Hauptverfasser: NAGAKURA, Naoki, SOUMA, Shinji, SHIMIZU, Tadayori, UNO, Katsuji, YANAGIHARA, Yasutake
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container_title Chemical & pharmaceutical bulletin
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creator NAGAKURA, Naoki
SOUMA, Shinji
SHIMIZU, Tadayori
UNO, Katsuji
YANAGIHARA, Yasutake
description The cross-reactivity of imipenem (IPM) in a delayed-type hypersensitivity (DTH) reaction was investigated by intradermal skin reaction, macrophage migration inhibition tests (MIT) and lymphocyte stimulation tests (LST) in guinea pigs. The animals were immunized with IPM, ampicillin (ABPC) or cephalexin (CEX) using Freund's complete adjuvant. Three sensitized-drugs exhibited the same immunogenicity in the skin reaction. The cross-reactivities in skin reaction among IPM, sulbactam, aztreonam, ABPC and 6-aminopenicillanic acid as penam, and CEX, ceftizoxime, 7-aminocephalosporanic acid as cephem were examined. IPM did not show cross-reactions with any of the tested drugs in three sensitized groups, indicating that the drugs possessed no cross-reactivity with tested beta-lactams in DTH.In MIT, 4 or 5 of 6 animals reacted to be sensitized drugs in each group. The cross-reactivity of IPM- and ABPC-sensitized groups in MIT was similar to that of a skin reaction, however, the CEX-sensitized animals showed broad cross-reactions. Using a kind of test drug, one or two animals in the ABPC-sensitized group showed migration enhancement, but IPM- or CEX-sensitized animals did not exhibit migration enhancement. In LST, most of the animals tested exhibited lymphocyte prolifration by sensitized drugs but a cross-reaction was scarcely observed. The above results suggest that among beta-lactams, IPM has a very low cross-reactivity. LST is considered to be more a useful assay than MIT for in vitro identification of causative drugs in animal models.
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The animals were immunized with IPM, ampicillin (ABPC) or cephalexin (CEX) using Freund's complete adjuvant. Three sensitized-drugs exhibited the same immunogenicity in the skin reaction. The cross-reactivities in skin reaction among IPM, sulbactam, aztreonam, ABPC and 6-aminopenicillanic acid as penam, and CEX, ceftizoxime, 7-aminocephalosporanic acid as cephem were examined. IPM did not show cross-reactions with any of the tested drugs in three sensitized groups, indicating that the drugs possessed no cross-reactivity with tested beta-lactams in DTH.In MIT, 4 or 5 of 6 animals reacted to be sensitized drugs in each group. The cross-reactivity of IPM- and ABPC-sensitized groups in MIT was similar to that of a skin reaction, however, the CEX-sensitized animals showed broad cross-reactions. Using a kind of test drug, one or two animals in the ABPC-sensitized group showed migration enhancement, but IPM- or CEX-sensitized animals did not exhibit migration enhancement. In LST, most of the animals tested exhibited lymphocyte prolifration by sensitized drugs but a cross-reaction was scarcely observed. The above results suggest that among beta-lactams, IPM has a very low cross-reactivity. LST is considered to be more a useful assay than MIT for in vitro identification of causative drugs in animal models.</description><identifier>ISSN: 0009-2363</identifier><identifier>EISSN: 1347-5223</identifier><identifier>DOI: 10.1248/cpb.39.765</identifier><identifier>PMID: 2070462</identifier><identifier>CODEN: CPBTAL</identifier><language>eng</language><publisher>Tokyo: The Pharmaceutical Society of Japan</publisher><subject>Animals ; Anti-Bacterial Agents - immunology ; Antibiotics. Antiinfectious agents. Antiparasitic agents ; beta-lactam ; Biological and medical sciences ; Cross Reactions - immunology ; delayed-type hypersensitivity ; Drug Hypersensitivity - immunology ; guinea pig ; Guinea Pigs ; Hypersensitivity, Delayed - immunology ; imipenem ; Imipenem - immunology ; intradermal skin test ; lymphocyte stimulation test ; macrophage migration inhibition test ; Male ; Medical sciences ; Pharmacology. 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Pharm. Bull.</addtitle><description>The cross-reactivity of imipenem (IPM) in a delayed-type hypersensitivity (DTH) reaction was investigated by intradermal skin reaction, macrophage migration inhibition tests (MIT) and lymphocyte stimulation tests (LST) in guinea pigs. The animals were immunized with IPM, ampicillin (ABPC) or cephalexin (CEX) using Freund's complete adjuvant. Three sensitized-drugs exhibited the same immunogenicity in the skin reaction. The cross-reactivities in skin reaction among IPM, sulbactam, aztreonam, ABPC and 6-aminopenicillanic acid as penam, and CEX, ceftizoxime, 7-aminocephalosporanic acid as cephem were examined. IPM did not show cross-reactions with any of the tested drugs in three sensitized groups, indicating that the drugs possessed no cross-reactivity with tested beta-lactams in DTH.In MIT, 4 or 5 of 6 animals reacted to be sensitized drugs in each group. The cross-reactivity of IPM- and ABPC-sensitized groups in MIT was similar to that of a skin reaction, however, the CEX-sensitized animals showed broad cross-reactions. Using a kind of test drug, one or two animals in the ABPC-sensitized group showed migration enhancement, but IPM- or CEX-sensitized animals did not exhibit migration enhancement. In LST, most of the animals tested exhibited lymphocyte prolifration by sensitized drugs but a cross-reaction was scarcely observed. The above results suggest that among beta-lactams, IPM has a very low cross-reactivity. LST is considered to be more a useful assay than MIT for in vitro identification of causative drugs in animal models.</description><subject>Animals</subject><subject>Anti-Bacterial Agents - immunology</subject><subject>Antibiotics. Antiinfectious agents. Antiparasitic agents</subject><subject>beta-lactam</subject><subject>Biological and medical sciences</subject><subject>Cross Reactions - immunology</subject><subject>delayed-type hypersensitivity</subject><subject>Drug Hypersensitivity - immunology</subject><subject>guinea pig</subject><subject>Guinea Pigs</subject><subject>Hypersensitivity, Delayed - immunology</subject><subject>imipenem</subject><subject>Imipenem - immunology</subject><subject>intradermal skin test</subject><subject>lymphocyte stimulation test</subject><subject>macrophage migration inhibition test</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Pharmacology. 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Antiinfectious agents. Antiparasitic agents</topic><topic>beta-lactam</topic><topic>Biological and medical sciences</topic><topic>Cross Reactions - immunology</topic><topic>delayed-type hypersensitivity</topic><topic>Drug Hypersensitivity - immunology</topic><topic>guinea pig</topic><topic>Guinea Pigs</topic><topic>Hypersensitivity, Delayed - immunology</topic><topic>imipenem</topic><topic>Imipenem - immunology</topic><topic>intradermal skin test</topic><topic>lymphocyte stimulation test</topic><topic>macrophage migration inhibition test</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Pharmacology. Drug treatments</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>NAGAKURA, Naoki</creatorcontrib><creatorcontrib>SOUMA, Shinji</creatorcontrib><creatorcontrib>SHIMIZU, Tadayori</creatorcontrib><creatorcontrib>UNO, Katsuji</creatorcontrib><creatorcontrib>YANAGIHARA, Yasutake</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>Neurosciences Abstracts</collection><collection>Nucleic Acids Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>Immunology Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Chemical &amp; pharmaceutical bulletin</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>NAGAKURA, Naoki</au><au>SOUMA, Shinji</au><au>SHIMIZU, Tadayori</au><au>UNO, Katsuji</au><au>YANAGIHARA, Yasutake</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Comparison of Cross-Reactivities of Imipenem and Other Beta-Lactam Antibiotics by Delayed-Type Hypersensitivity Reaction in Guinea Pigs</atitle><jtitle>Chemical &amp; pharmaceutical bulletin</jtitle><addtitle>Chem. Pharm. Bull.</addtitle><date>1991</date><risdate>1991</risdate><volume>39</volume><issue>3</issue><spage>765</spage><epage>768</epage><pages>765-768</pages><issn>0009-2363</issn><eissn>1347-5223</eissn><coden>CPBTAL</coden><abstract>The cross-reactivity of imipenem (IPM) in a delayed-type hypersensitivity (DTH) reaction was investigated by intradermal skin reaction, macrophage migration inhibition tests (MIT) and lymphocyte stimulation tests (LST) in guinea pigs. The animals were immunized with IPM, ampicillin (ABPC) or cephalexin (CEX) using Freund's complete adjuvant. Three sensitized-drugs exhibited the same immunogenicity in the skin reaction. The cross-reactivities in skin reaction among IPM, sulbactam, aztreonam, ABPC and 6-aminopenicillanic acid as penam, and CEX, ceftizoxime, 7-aminocephalosporanic acid as cephem were examined. IPM did not show cross-reactions with any of the tested drugs in three sensitized groups, indicating that the drugs possessed no cross-reactivity with tested beta-lactams in DTH.In MIT, 4 or 5 of 6 animals reacted to be sensitized drugs in each group. The cross-reactivity of IPM- and ABPC-sensitized groups in MIT was similar to that of a skin reaction, however, the CEX-sensitized animals showed broad cross-reactions. Using a kind of test drug, one or two animals in the ABPC-sensitized group showed migration enhancement, but IPM- or CEX-sensitized animals did not exhibit migration enhancement. In LST, most of the animals tested exhibited lymphocyte prolifration by sensitized drugs but a cross-reaction was scarcely observed. The above results suggest that among beta-lactams, IPM has a very low cross-reactivity. LST is considered to be more a useful assay than MIT for in vitro identification of causative drugs in animal models.</abstract><cop>Tokyo</cop><pub>The Pharmaceutical Society of Japan</pub><pmid>2070462</pmid><doi>10.1248/cpb.39.765</doi><tpages>4</tpages><oa>free_for_read</oa></addata></record>
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subjects Animals
Anti-Bacterial Agents - immunology
Antibiotics. Antiinfectious agents. Antiparasitic agents
beta-lactam
Biological and medical sciences
Cross Reactions - immunology
delayed-type hypersensitivity
Drug Hypersensitivity - immunology
guinea pig
Guinea Pigs
Hypersensitivity, Delayed - immunology
imipenem
Imipenem - immunology
intradermal skin test
lymphocyte stimulation test
macrophage migration inhibition test
Male
Medical sciences
Pharmacology. Drug treatments
title Comparison of Cross-Reactivities of Imipenem and Other Beta-Lactam Antibiotics by Delayed-Type Hypersensitivity Reaction in Guinea Pigs
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