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Elicitation of homologous passive cutaneous anaphylactic reactions by a benzylpenicillin preparation

Identifieur interne : 003863 ( Istex/Corpus ); précédent : 003862; suivant : 003864

Elicitation of homologous passive cutaneous anaphylactic reactions by a benzylpenicillin preparation

Auteurs : Masaharu Muranaka ; Hiroshi Igarashi ; Kazuhiro Koizumi ; Hiroshi Okumura ; Koyo Takeda ; Shuji Suzuki

Source :

RBID : ISTEX:ADF98802F42C8AC7FE8F5AC2F95038E5BA398022

Abstract

Four out of five commercially available benzylpenicillin preparations elicited homologous passive cutaneous anaphylactic (PCA) reaction in sensitized guinea pigs with anti-benzylpenicilloyl (anti-BPO) reaginic sera. The same preparations could not evoke PCA reaction in sensitized guinea pigs with anti-BPO γ1 homocytotropic antibodies. The PCA reactions were completely inhibited by a prior injection of BPO-ε-aminocaproic acid (BPO-EACA). Chromatographic analysis of one of the benzylpenicillin preparations on Sephadex G 10 revealed that the reagin-mediated PCA reaction was not evoked with the fractions from the main peak of the benzylpenicillin but with fractions eluted earlier. None of the fractions gave positive γ1-mediated PCA reactions. These results indicated that some commercial benzylpenicillin preparations contained minute amounts of the impurities that could elicit the homologous PCA reaction in guinea pigs sensitized with anti-BPO reaginic sera. It was also indicated that the PCA elicitation activity of the benzylpenicillin preparation in the system of reagin-mediated PCA differed from that of γ1-mediated PCA.

Url:
DOI: 10.1016/0091-6749(74)90023-2

Links to Exploration step

ISTEX:ADF98802F42C8AC7FE8F5AC2F95038E5BA398022

Le document en format XML

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<div type="abstract" xml:lang="en">Four out of five commercially available benzylpenicillin preparations elicited homologous passive cutaneous anaphylactic (PCA) reaction in sensitized guinea pigs with anti-benzylpenicilloyl (anti-BPO) reaginic sera. The same preparations could not evoke PCA reaction in sensitized guinea pigs with anti-BPO γ1 homocytotropic antibodies. The PCA reactions were completely inhibited by a prior injection of BPO-ε-aminocaproic acid (BPO-EACA). Chromatographic analysis of one of the benzylpenicillin preparations on Sephadex G 10 revealed that the reagin-mediated PCA reaction was not evoked with the fractions from the main peak of the benzylpenicillin but with fractions eluted earlier. None of the fractions gave positive γ1-mediated PCA reactions. These results indicated that some commercial benzylpenicillin preparations contained minute amounts of the impurities that could elicit the homologous PCA reaction in guinea pigs sensitized with anti-BPO reaginic sera. It was also indicated that the PCA elicitation activity of the benzylpenicillin preparation in the system of reagin-mediated PCA differed from that of γ1-mediated PCA.</div>
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<term>BPO</term>
<term>benzylpenicilloyl</term>
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<term>PcG</term>
<term>benzylpenicillin preparation</term>
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<item>
<term>BPE</term>
<term>benzylpenicillenic acid</term>
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<item>
<term>BPOA</term>
<term>bonzylpenicilloic acid</term>
</item>
<item>
<term>EACA</term>
<term>ϵ-aminoeaproic acid BSA bovine serum albumin</term>
</item>
<item>
<term>BGG</term>
<term>bovine gamma globulin GP guinea pig</term>
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<term>GSP</term>
<term>guinea pig serum protein</term>
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<ce:text>Reprint requests to: Dr. Masaharu Muranaka, Department of Medicine and Physical Therapy, Faculty of Medicine, University of Tokyo, 7-3-1 Hongo, Bunkyo-ku, Tokyo, Japan.</ce:text>
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<ce:simple-para>Four out of five commercially available benzylpenicillin preparations elicited homologous passive cutaneous anaphylactic (PCA) reaction in sensitized guinea pigs with anti-benzylpenicilloyl (anti-BPO) reaginic sera. The same preparations could not evoke PCA reaction in sensitized guinea pigs with anti-BPO
<ce:italic>γ</ce:italic>
<ce:inf>1</ce:inf>
homocytotropic antibodies. The PCA reactions were completely inhibited by a prior injection of BPO-ε-aminocaproic acid (BPO-EACA). Chromatographic analysis of one of the benzylpenicillin preparations on Sephadex G 10 revealed that the reagin-mediated PCA reaction was not evoked with the fractions from the main peak of the benzylpenicillin but with fractions eluted earlier. None of the fractions gave positive
<ce:italic>γ</ce:italic>
<ce:inf>1</ce:inf>
-mediated PCA reactions. These results indicated that some commercial benzylpenicillin preparations contained minute amounts of the impurities that could elicit the homologous PCA reaction in guinea pigs sensitized with anti-BPO reaginic sera. It was also indicated that the PCA elicitation activity of the benzylpenicillin preparation in the system of reagin-mediated PCA differed from that of
<ce:italic>γ</ce:italic>
<ce:inf>1</ce:inf>
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<ce:text>PCA</ce:text>
<ce:keyword>
<ce:text>passive cutaneous anaphylaxis</ce:text>
</ce:keyword>
</ce:keyword>
<ce:keyword>
<ce:text>BPO</ce:text>
<ce:keyword>
<ce:text>benzylpenicilloyl</ce:text>
</ce:keyword>
</ce:keyword>
<ce:keyword>
<ce:text>PcG</ce:text>
<ce:keyword>
<ce:text>benzylpenicillin preparation</ce:text>
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</ce:keyword>
<ce:keyword>
<ce:text>BPE</ce:text>
<ce:keyword>
<ce:text>benzylpenicillenic acid</ce:text>
</ce:keyword>
</ce:keyword>
<ce:keyword>
<ce:text>BPOA</ce:text>
<ce:keyword>
<ce:text>bonzylpenicilloic acid</ce:text>
</ce:keyword>
</ce:keyword>
<ce:keyword>
<ce:text>EACA</ce:text>
<ce:keyword>
<ce:text>ϵ-aminoeaproic acid BSA bovine serum albumin</ce:text>
</ce:keyword>
</ce:keyword>
<ce:keyword>
<ce:text>BGG</ce:text>
<ce:keyword>
<ce:text>bovine gamma globulin GP guinea pig</ce:text>
</ce:keyword>
</ce:keyword>
<ce:keyword>
<ce:text>GSP</ce:text>
<ce:keyword>
<ce:text>guinea pig serum protein</ce:text>
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<title>Elicitation of homologous passive cutaneous anaphylactic reactions by a benzylpenicillin preparation</title>
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<title>Elicitation of homologous passive cutaneous anaphylactic reactions by a benzylpenicillin preparation</title>
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<name type="personal">
<namePart type="given">Masaharu</namePart>
<namePart type="family">Muranaka</namePart>
<affiliation>From the Department of Medicine and Physical Therapy, Faculty of Medicine, University of Tokyo Tokyo, Japan</affiliation>
<description>Reprint requests to: Dr. Masaharu Muranaka, Department of Medicine and Physical Therapy, Faculty of Medicine, University of Tokyo, 7-3-1 Hongo, Bunkyo-ku, Tokyo, Japan.</description>
<role>
<roleTerm type="text">author</roleTerm>
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<name type="personal">
<namePart type="given">Hiroshi</namePart>
<namePart type="family">Igarashi</namePart>
<affiliation>From the Department of Medicine and Physical Therapy, Faculty of Medicine, University of Tokyo Tokyo, Japan</affiliation>
<role>
<roleTerm type="text">author</roleTerm>
</role>
</name>
<name type="personal">
<namePart type="given">Kazuhiro</namePart>
<namePart type="family">Koizumi</namePart>
<affiliation>From the Department of Medicine and Physical Therapy, Faculty of Medicine, University of Tokyo Tokyo, Japan</affiliation>
<role>
<roleTerm type="text">author</roleTerm>
</role>
</name>
<name type="personal">
<namePart type="given">Hiroshi</namePart>
<namePart type="family">Okumura</namePart>
<affiliation>From the Department of Medicine and Physical Therapy, Faculty of Medicine, University of Tokyo Tokyo, Japan</affiliation>
<role>
<roleTerm type="text">author</roleTerm>
</role>
</name>
<name type="personal">
<namePart type="given">Koyo</namePart>
<namePart type="family">Takeda</namePart>
<affiliation>From the Department of Medicine and Physical Therapy, Faculty of Medicine, University of Tokyo Tokyo, Japan</affiliation>
<role>
<roleTerm type="text">author</roleTerm>
</role>
</name>
<name type="personal">
<namePart type="given">Shuji</namePart>
<namePart type="family">Suzuki</namePart>
<affiliation>From the Department of Medicine and Physical Therapy, Faculty of Medicine, University of Tokyo Tokyo, Japan</affiliation>
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<dateIssued encoding="w3cdtf">1973</dateIssued>
<dateCaptured encoding="w3cdtf">1973-12-13</dateCaptured>
<copyrightDate encoding="w3cdtf">1974</copyrightDate>
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<abstract lang="en">Four out of five commercially available benzylpenicillin preparations elicited homologous passive cutaneous anaphylactic (PCA) reaction in sensitized guinea pigs with anti-benzylpenicilloyl (anti-BPO) reaginic sera. The same preparations could not evoke PCA reaction in sensitized guinea pigs with anti-BPO γ1 homocytotropic antibodies. The PCA reactions were completely inhibited by a prior injection of BPO-ε-aminocaproic acid (BPO-EACA). Chromatographic analysis of one of the benzylpenicillin preparations on Sephadex G 10 revealed that the reagin-mediated PCA reaction was not evoked with the fractions from the main peak of the benzylpenicillin but with fractions eluted earlier. None of the fractions gave positive γ1-mediated PCA reactions. These results indicated that some commercial benzylpenicillin preparations contained minute amounts of the impurities that could elicit the homologous PCA reaction in guinea pigs sensitized with anti-BPO reaginic sera. It was also indicated that the PCA elicitation activity of the benzylpenicillin preparation in the system of reagin-mediated PCA differed from that of γ1-mediated PCA.</abstract>
<subject>
<genre>Abbreviations</genre>
<topic>PCA : passive cutaneous anaphylaxis</topic>
<topic>BPO : benzylpenicilloyl</topic>
<topic>PcG : benzylpenicillin preparation</topic>
<topic>BPE : benzylpenicillenic acid</topic>
<topic>BPOA : bonzylpenicilloic acid</topic>
<topic>EACA : ϵ-aminoeaproic acid BSA bovine serum albumin</topic>
<topic>BGG : bovine gamma globulin GP guinea pig</topic>
<topic>GSP : guinea pig serum protein</topic>
</subject>
<relatedItem type="host">
<titleInfo>
<title>The Journal of Allergy and Clinical Immunology</title>
</titleInfo>
<titleInfo type="abbreviated">
<title>YMAI</title>
</titleInfo>
<genre type="Journal">journal</genre>
<originInfo>
<dateIssued encoding="w3cdtf">197412</dateIssued>
</originInfo>
<identifier type="ISSN">0091-6749</identifier>
<identifier type="PII">S0091-6749(00)X0119-4</identifier>
<part>
<date>197412</date>
<detail type="volume">
<number>54</number>
<caption>vol.</caption>
</detail>
<detail type="issue">
<number>6</number>
<caption>no.</caption>
</detail>
<extent unit="issue pages">
<start>A39</start>
<end>A46</end>
</extent>
<extent unit="issue pages">
<start>2</start>
<end>412</end>
</extent>
<extent unit="pages">
<start>329</start>
<end>338</end>
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</relatedItem>
<identifier type="istex">ADF98802F42C8AC7FE8F5AC2F95038E5BA398022</identifier>
<identifier type="DOI">10.1016/0091-6749(74)90023-2</identifier>
<identifier type="PII">0091-6749(74)90023-2</identifier>
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