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Food Allergy Herbal Formula-2 silences peanut-induced anaphylaxis for a prolonged posttreatment period via IFN-γ–producing CD8+ T cells
Background Food allergy is a serious and sometimes fatal condition for which there is no cure. We previously reported that Food Allergy Herbal Formula (FAHF)–2) protected peanut-allergic mice against anaphylactic reactions as long as 4 weeks posttherapy. This formula is now in clinical trials in the...
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Published in: | Journal of allergy and clinical immunology 2009-02, Vol.123 (2), p.443-451 |
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description | Background Food allergy is a serious and sometimes fatal condition for which there is no cure. We previously reported that Food Allergy Herbal Formula (FAHF)–2) protected peanut-allergic mice against anaphylactic reactions as long as 4 weeks posttherapy. This formula is now in clinical trials in the United States. Objective We sought to determine whether FAHF-2–mediated protection could be extended long-term and explored the mechanisms underlying its persistent immunomodulatory effects. Methods Peanut-allergic mice received FAHF-2 daily orally by gavage for 7 weeks, and then received 7 oral peanut challenges at intervals of 4 to 10 weeks over a period of 36 weeks. For mechanistic studies, some mice received CD4+ or CD8+ T-cell–depleting antibodies or IFN-γ–neutralizing antibodies. Anaphylactic symptoms, body temperatures, and plasma histamine levels were recorded after each challenge, and peanut-specific immunoglobulin levels and cytokine profiles of splenocytes, mesenteric lymph node cells, and purified CD4+ and CD8+ T cells were determined. Results Food Allergy Herbal Formula-2 treatment protected mice from anaphylaxis for more than 36 weeks after discontinuing treatment. Peanut-specific IgE levels were reduced as much as 50%, whereas IgG2a levels were increased as much as 60%, and these effects persisted over time. TH 2 cytokine production by CD4+ T cells from FAHF-2–treated mice was reduced as much as 75%, whereas CD8+ T-cell IFN-γ production was markedly increased by as much as 85% at the final challenge. Neutralization of INF-γ and depletion of CD8+ T cells markedly attenuated FAHF-2 efficacy. Conclusions Food Allergy Herbal Formula-2 provides long-term protection from anaphylaxis by inducing a beneficial shift in allergen-specific immune responses mediated largely by elevated CD8+ T-cell IFN-γ production. |
doi_str_mv | 10.1016/j.jaci.2008.12.1107 |
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We previously reported that Food Allergy Herbal Formula (FAHF)–2) protected peanut-allergic mice against anaphylactic reactions as long as 4 weeks posttherapy. This formula is now in clinical trials in the United States. Objective We sought to determine whether FAHF-2–mediated protection could be extended long-term and explored the mechanisms underlying its persistent immunomodulatory effects. Methods Peanut-allergic mice received FAHF-2 daily orally by gavage for 7 weeks, and then received 7 oral peanut challenges at intervals of 4 to 10 weeks over a period of 36 weeks. For mechanistic studies, some mice received CD4+ or CD8+ T-cell–depleting antibodies or IFN-γ–neutralizing antibodies. Anaphylactic symptoms, body temperatures, and plasma histamine levels were recorded after each challenge, and peanut-specific immunoglobulin levels and cytokine profiles of splenocytes, mesenteric lymph node cells, and purified CD4+ and CD8+ T cells were determined. Results Food Allergy Herbal Formula-2 treatment protected mice from anaphylaxis for more than 36 weeks after discontinuing treatment. Peanut-specific IgE levels were reduced as much as 50%, whereas IgG2a levels were increased as much as 60%, and these effects persisted over time. TH 2 cytokine production by CD4+ T cells from FAHF-2–treated mice was reduced as much as 75%, whereas CD8+ T-cell IFN-γ production was markedly increased by as much as 85% at the final challenge. Neutralization of INF-γ and depletion of CD8+ T cells markedly attenuated FAHF-2 efficacy. Conclusions Food Allergy Herbal Formula-2 provides long-term protection from anaphylaxis by inducing a beneficial shift in allergen-specific immune responses mediated largely by elevated CD8+ T-cell IFN-γ production.</description><identifier>ISSN: 0091-6749</identifier><identifier>EISSN: 1097-6825</identifier><identifier>DOI: 10.1016/j.jaci.2008.12.1107</identifier><identifier>PMID: 19203662</identifier><identifier>CODEN: JACIBY</identifier><language>eng</language><publisher>New York, NY: Mosby, Inc</publisher><subject>Allergens - administration & dosage ; Allergens - immunology ; Allergens - pharmacology ; Allergy and Immunology ; anaphylaxis ; Anaphylaxis - immunology ; Anaphylaxis - prevention & control ; Animals ; Arachis - immunology ; Arachis hypogaea ; Biological and medical sciences ; CD4-Positive T-Lymphocytes - drug effects ; CD4-Positive T-Lymphocytes - immunology ; CD4-Positive T-Lymphocytes - metabolism ; CD8 ; CD8-Positive T-Lymphocytes - drug effects ; CD8-Positive T-Lymphocytes - immunology ; CD8-Positive T-Lymphocytes - metabolism ; Cytokines - biosynthesis ; Cytokines - drug effects ; Cytokines - immunology ; Disease Models, Animal ; Female ; Fundamental and applied biological sciences. Psychology ; Fundamental immunology ; Histamine - blood ; IgE ; Immunoglobulin E - blood ; Interferon-gamma - immunology ; Interferon-gamma - metabolism ; Lymphocyte Depletion ; Medical sciences ; Mice ; Mice, Inbred C3H ; murine model ; Peanut allergy ; Peanut Hypersensitivity - immunology ; Peanut Hypersensitivity - prevention & control ; Plant Extracts - pharmacology ; Plant Extracts - therapeutic use ; Sarcoidosis. Granulomatous diseases of unproved etiology. Connective tissue diseases. Elastic tissue diseases. Vasculitis ; T cells ; T H2 cytokines ; Th2 Cells - drug effects ; Th2 Cells - immunology ; Th2 Cells - metabolism ; traditional Chinese herbal medicine</subject><ispartof>Journal of allergy and clinical immunology, 2009-02, Vol.123 (2), p.443-451</ispartof><rights>American Academy of Allergy, Asthma & Immunology</rights><rights>2009 American Academy of Allergy, Asthma & Immunology</rights><rights>2009 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c473t-2a6bf973105e82a23a303f6216415b920d580a6e3c01005b9b722bfedb1a6f0d3</citedby><cites>FETCH-LOGICAL-c473t-2a6bf973105e82a23a303f6216415b920d580a6e3c01005b9b722bfedb1a6f0d3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27923,27924</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=21126802$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/19203662$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Srivastava, Kamal D., MPhil</creatorcontrib><creatorcontrib>Qu, Chunfeng, MD, PhD</creatorcontrib><creatorcontrib>Zhang, Tengfei, PhD</creatorcontrib><creatorcontrib>Goldfarb, Joseph, PhD</creatorcontrib><creatorcontrib>Sampson, Hugh A., MD</creatorcontrib><creatorcontrib>Li, Xiu-Min, MD</creatorcontrib><title>Food Allergy Herbal Formula-2 silences peanut-induced anaphylaxis for a prolonged posttreatment period via IFN-γ–producing CD8+ T cells</title><title>Journal of allergy and clinical immunology</title><addtitle>J Allergy Clin Immunol</addtitle><description>Background Food allergy is a serious and sometimes fatal condition for which there is no cure. We previously reported that Food Allergy Herbal Formula (FAHF)–2) protected peanut-allergic mice against anaphylactic reactions as long as 4 weeks posttherapy. This formula is now in clinical trials in the United States. Objective We sought to determine whether FAHF-2–mediated protection could be extended long-term and explored the mechanisms underlying its persistent immunomodulatory effects. Methods Peanut-allergic mice received FAHF-2 daily orally by gavage for 7 weeks, and then received 7 oral peanut challenges at intervals of 4 to 10 weeks over a period of 36 weeks. For mechanistic studies, some mice received CD4+ or CD8+ T-cell–depleting antibodies or IFN-γ–neutralizing antibodies. Anaphylactic symptoms, body temperatures, and plasma histamine levels were recorded after each challenge, and peanut-specific immunoglobulin levels and cytokine profiles of splenocytes, mesenteric lymph node cells, and purified CD4+ and CD8+ T cells were determined. Results Food Allergy Herbal Formula-2 treatment protected mice from anaphylaxis for more than 36 weeks after discontinuing treatment. Peanut-specific IgE levels were reduced as much as 50%, whereas IgG2a levels were increased as much as 60%, and these effects persisted over time. TH 2 cytokine production by CD4+ T cells from FAHF-2–treated mice was reduced as much as 75%, whereas CD8+ T-cell IFN-γ production was markedly increased by as much as 85% at the final challenge. Neutralization of INF-γ and depletion of CD8+ T cells markedly attenuated FAHF-2 efficacy. Conclusions Food Allergy Herbal Formula-2 provides long-term protection from anaphylaxis by inducing a beneficial shift in allergen-specific immune responses mediated largely by elevated CD8+ T-cell IFN-γ production.</description><subject>Allergens - administration & dosage</subject><subject>Allergens - immunology</subject><subject>Allergens - pharmacology</subject><subject>Allergy and Immunology</subject><subject>anaphylaxis</subject><subject>Anaphylaxis - immunology</subject><subject>Anaphylaxis - prevention & control</subject><subject>Animals</subject><subject>Arachis - immunology</subject><subject>Arachis hypogaea</subject><subject>Biological and medical sciences</subject><subject>CD4-Positive T-Lymphocytes - drug effects</subject><subject>CD4-Positive T-Lymphocytes - immunology</subject><subject>CD4-Positive T-Lymphocytes - metabolism</subject><subject>CD8</subject><subject>CD8-Positive T-Lymphocytes - drug effects</subject><subject>CD8-Positive T-Lymphocytes - immunology</subject><subject>CD8-Positive T-Lymphocytes - metabolism</subject><subject>Cytokines - biosynthesis</subject><subject>Cytokines - drug effects</subject><subject>Cytokines - immunology</subject><subject>Disease Models, Animal</subject><subject>Female</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Fundamental immunology</subject><subject>Histamine - blood</subject><subject>IgE</subject><subject>Immunoglobulin E - blood</subject><subject>Interferon-gamma - immunology</subject><subject>Interferon-gamma - metabolism</subject><subject>Lymphocyte Depletion</subject><subject>Medical sciences</subject><subject>Mice</subject><subject>Mice, Inbred C3H</subject><subject>murine model</subject><subject>Peanut allergy</subject><subject>Peanut Hypersensitivity - immunology</subject><subject>Peanut Hypersensitivity - prevention & control</subject><subject>Plant Extracts - pharmacology</subject><subject>Plant Extracts - therapeutic use</subject><subject>Sarcoidosis. Granulomatous diseases of unproved etiology. Connective tissue diseases. Elastic tissue diseases. Vasculitis</subject><subject>T cells</subject><subject>T H2 cytokines</subject><subject>Th2 Cells - drug effects</subject><subject>Th2 Cells - immunology</subject><subject>Th2 Cells - metabolism</subject><subject>traditional Chinese herbal medicine</subject><issn>0091-6749</issn><issn>1097-6825</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2009</creationdate><recordtype>article</recordtype><recordid>eNqFksGO0zAQhiMEYpeFJ0BCvsAFpYzt1kkOIK0KZVdawYHlbE2cSXFx7WInK3rjzJVH4T14CJ4ER61A4rIny57vnxnPP0XxmMOMA1cvNrMNGjsTAPWMixnnUN0pTjk0ValqsbhbnAI0vFTVvDkpHqS0gXyXdXO_OOGNAKmUOC2-r0Lo2LlzFNd7dkGxRcdWIW5Hh6VgyTryhhLbEfpxKK3vRkMdQ4-7T3uHX21ifYgM2S4GF_w6x3YhDUMkHLbkhyyMNle4scguV-_KXz9_f_uR2ZzG-jVbvq6fs2tmyLn0sLjXo0v06HieFR9Xb66XF-XV-7eXy_Or0swrOZQCVds3leSwoFqgkChB9kpwNeeLNn-sW9SAiqQBDpBf2kqItqeu5ah66ORZ8eyQN7fxZaQ06K1NUwfoKYxJK9WA4ILfCuYZNkpUKoPyAJoYUorU6120W4x7zUFPXumNnrzSk1eaCz15lVVPjunHdkvdP83RnAw8PQKYDLo-ojc2_eUE50LVMHEvDxzlqd1YijoZO9nW2Uhm0F2wtzTy6j-9cdbbXPIz7Sltwhh9NkRznYQG_WFaq2mroAY5V5WQfwB0d8jn</recordid><startdate>20090201</startdate><enddate>20090201</enddate><creator>Srivastava, Kamal D., MPhil</creator><creator>Qu, Chunfeng, MD, PhD</creator><creator>Zhang, Tengfei, PhD</creator><creator>Goldfarb, Joseph, PhD</creator><creator>Sampson, Hugh A., MD</creator><creator>Li, Xiu-Min, MD</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>7T5</scope><scope>H94</scope><scope>7X8</scope></search><sort><creationdate>20090201</creationdate><title>Food Allergy Herbal Formula-2 silences peanut-induced anaphylaxis for a prolonged posttreatment period via IFN-γ–producing CD8+ T cells</title><author>Srivastava, Kamal D., MPhil ; Qu, Chunfeng, MD, PhD ; Zhang, Tengfei, PhD ; Goldfarb, Joseph, PhD ; Sampson, Hugh A., MD ; Li, Xiu-Min, MD</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c473t-2a6bf973105e82a23a303f6216415b920d580a6e3c01005b9b722bfedb1a6f0d3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2009</creationdate><topic>Allergens - administration & dosage</topic><topic>Allergens - immunology</topic><topic>Allergens - pharmacology</topic><topic>Allergy and Immunology</topic><topic>anaphylaxis</topic><topic>Anaphylaxis - immunology</topic><topic>Anaphylaxis - prevention & control</topic><topic>Animals</topic><topic>Arachis - immunology</topic><topic>Arachis hypogaea</topic><topic>Biological and medical sciences</topic><topic>CD4-Positive T-Lymphocytes - drug effects</topic><topic>CD4-Positive T-Lymphocytes - immunology</topic><topic>CD4-Positive T-Lymphocytes - metabolism</topic><topic>CD8</topic><topic>CD8-Positive T-Lymphocytes - drug effects</topic><topic>CD8-Positive T-Lymphocytes - immunology</topic><topic>CD8-Positive T-Lymphocytes - metabolism</topic><topic>Cytokines - biosynthesis</topic><topic>Cytokines - drug effects</topic><topic>Cytokines - immunology</topic><topic>Disease Models, Animal</topic><topic>Female</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Fundamental immunology</topic><topic>Histamine - blood</topic><topic>IgE</topic><topic>Immunoglobulin E - blood</topic><topic>Interferon-gamma - immunology</topic><topic>Interferon-gamma - metabolism</topic><topic>Lymphocyte Depletion</topic><topic>Medical sciences</topic><topic>Mice</topic><topic>Mice, Inbred C3H</topic><topic>murine model</topic><topic>Peanut allergy</topic><topic>Peanut Hypersensitivity - immunology</topic><topic>Peanut Hypersensitivity - prevention & control</topic><topic>Plant Extracts - pharmacology</topic><topic>Plant Extracts - therapeutic use</topic><topic>Sarcoidosis. Granulomatous diseases of unproved etiology. Connective tissue diseases. Elastic tissue diseases. Vasculitis</topic><topic>T cells</topic><topic>T H2 cytokines</topic><topic>Th2 Cells - drug effects</topic><topic>Th2 Cells - immunology</topic><topic>Th2 Cells - metabolism</topic><topic>traditional Chinese herbal medicine</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Srivastava, Kamal D., MPhil</creatorcontrib><creatorcontrib>Qu, Chunfeng, MD, PhD</creatorcontrib><creatorcontrib>Zhang, Tengfei, PhD</creatorcontrib><creatorcontrib>Goldfarb, Joseph, PhD</creatorcontrib><creatorcontrib>Sampson, Hugh A., MD</creatorcontrib><creatorcontrib>Li, Xiu-Min, MD</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>Immunology Abstracts</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of allergy and clinical immunology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Srivastava, Kamal D., MPhil</au><au>Qu, Chunfeng, MD, PhD</au><au>Zhang, Tengfei, PhD</au><au>Goldfarb, Joseph, PhD</au><au>Sampson, Hugh A., MD</au><au>Li, Xiu-Min, MD</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Food Allergy Herbal Formula-2 silences peanut-induced anaphylaxis for a prolonged posttreatment period via IFN-γ–producing CD8+ T cells</atitle><jtitle>Journal of allergy and clinical immunology</jtitle><addtitle>J Allergy Clin Immunol</addtitle><date>2009-02-01</date><risdate>2009</risdate><volume>123</volume><issue>2</issue><spage>443</spage><epage>451</epage><pages>443-451</pages><issn>0091-6749</issn><eissn>1097-6825</eissn><coden>JACIBY</coden><abstract>Background Food allergy is a serious and sometimes fatal condition for which there is no cure. We previously reported that Food Allergy Herbal Formula (FAHF)–2) protected peanut-allergic mice against anaphylactic reactions as long as 4 weeks posttherapy. This formula is now in clinical trials in the United States. Objective We sought to determine whether FAHF-2–mediated protection could be extended long-term and explored the mechanisms underlying its persistent immunomodulatory effects. Methods Peanut-allergic mice received FAHF-2 daily orally by gavage for 7 weeks, and then received 7 oral peanut challenges at intervals of 4 to 10 weeks over a period of 36 weeks. For mechanistic studies, some mice received CD4+ or CD8+ T-cell–depleting antibodies or IFN-γ–neutralizing antibodies. Anaphylactic symptoms, body temperatures, and plasma histamine levels were recorded after each challenge, and peanut-specific immunoglobulin levels and cytokine profiles of splenocytes, mesenteric lymph node cells, and purified CD4+ and CD8+ T cells were determined. Results Food Allergy Herbal Formula-2 treatment protected mice from anaphylaxis for more than 36 weeks after discontinuing treatment. Peanut-specific IgE levels were reduced as much as 50%, whereas IgG2a levels were increased as much as 60%, and these effects persisted over time. TH 2 cytokine production by CD4+ T cells from FAHF-2–treated mice was reduced as much as 75%, whereas CD8+ T-cell IFN-γ production was markedly increased by as much as 85% at the final challenge. Neutralization of INF-γ and depletion of CD8+ T cells markedly attenuated FAHF-2 efficacy. Conclusions Food Allergy Herbal Formula-2 provides long-term protection from anaphylaxis by inducing a beneficial shift in allergen-specific immune responses mediated largely by elevated CD8+ T-cell IFN-γ production.</abstract><cop>New York, NY</cop><pub>Mosby, Inc</pub><pmid>19203662</pmid><doi>10.1016/j.jaci.2008.12.1107</doi><tpages>9</tpages></addata></record> |
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subjects | Allergens - administration & dosage Allergens - immunology Allergens - pharmacology Allergy and Immunology anaphylaxis Anaphylaxis - immunology Anaphylaxis - prevention & control Animals Arachis - immunology Arachis hypogaea Biological and medical sciences CD4-Positive T-Lymphocytes - drug effects CD4-Positive T-Lymphocytes - immunology CD4-Positive T-Lymphocytes - metabolism CD8 CD8-Positive T-Lymphocytes - drug effects CD8-Positive T-Lymphocytes - immunology CD8-Positive T-Lymphocytes - metabolism Cytokines - biosynthesis Cytokines - drug effects Cytokines - immunology Disease Models, Animal Female Fundamental and applied biological sciences. Psychology Fundamental immunology Histamine - blood IgE Immunoglobulin E - blood Interferon-gamma - immunology Interferon-gamma - metabolism Lymphocyte Depletion Medical sciences Mice Mice, Inbred C3H murine model Peanut allergy Peanut Hypersensitivity - immunology Peanut Hypersensitivity - prevention & control Plant Extracts - pharmacology Plant Extracts - therapeutic use Sarcoidosis. Granulomatous diseases of unproved etiology. Connective tissue diseases. Elastic tissue diseases. Vasculitis T cells T H2 cytokines Th2 Cells - drug effects Th2 Cells - immunology Th2 Cells - metabolism traditional Chinese herbal medicine |
title | Food Allergy Herbal Formula-2 silences peanut-induced anaphylaxis for a prolonged posttreatment period via IFN-γ–producing CD8+ T cells |
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