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Neem leaf glycoprotein directs T-bet–associated type 1 immune commitment
Abstract Neem leaf glycoprotein (NLGP)–mediated immune activation and associated immune polarization was studied. NLGP–induced activation is reflected in upregulation of early activation marker CD69 on lymphocytes, monocytes, and dendritic cells. Activation is also denoted by CD45RO enhancement, wit...
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Published in: | Human immunology 2009, Vol.70 (1), p.6-15 |
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creator | Bose, Anamika Chakraborty, Krishnendu Sarkar, Koustav Goswami, Shyamal Haque, Enamul Chakraborty, Tathagata Ghosh, Diptendu Roy, Soumyabrata Laskar, Subrata Baral, Rathindranath |
description | Abstract Neem leaf glycoprotein (NLGP)–mediated immune activation and associated immune polarization was studied. NLGP–induced activation is reflected in upregulation of early activation marker CD69 on lymphocytes, monocytes, and dendritic cells. Activation is also denoted by CD45RO enhancement, with a decrease in CD45RA phenotype and CD62L (L-selectin). NLGP-activated T cells secrete greater amount of signature T-helper (Th)1 cytokines interferon-γ and a lower amount of the Th2 cytokine interleukin (IL)–4. Similar type 1 directiveness is also observed in antigen-presenting monocytes and dendritic cells by upregulation of IL-12, tumor necrosis factor –α and downregulation of IL-10. Creation of the type 1 microenvironment is also assisted by NLGP-induced downregulation of FoxP3+ T-Reg cells. A type 1–specific transcription factor, T-bet, is upregulated in circulating immune cells after their stimulation with NLGP. In the creation of type 1 immune network, increased phosphorylation of STAT1 and STAT4 with decreased phosphorylation of STAT3 might have significance. We conclude that NLGP may be effective in maintaining normal immune homeostasis by upregulating type 1 response in immunosuppressed hosts, which may have significant role in the induction of host protective antitumor functions. |
doi_str_mv | 10.1016/j.humimm.2008.09.004 |
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NLGP–induced activation is reflected in upregulation of early activation marker CD69 on lymphocytes, monocytes, and dendritic cells. Activation is also denoted by CD45RO enhancement, with a decrease in CD45RA phenotype and CD62L (L-selectin). NLGP-activated T cells secrete greater amount of signature T-helper (Th)1 cytokines interferon-γ and a lower amount of the Th2 cytokine interleukin (IL)–4. Similar type 1 directiveness is also observed in antigen-presenting monocytes and dendritic cells by upregulation of IL-12, tumor necrosis factor –α and downregulation of IL-10. Creation of the type 1 microenvironment is also assisted by NLGP-induced downregulation of FoxP3+ T-Reg cells. A type 1–specific transcription factor, T-bet, is upregulated in circulating immune cells after their stimulation with NLGP. In the creation of type 1 immune network, increased phosphorylation of STAT1 and STAT4 with decreased phosphorylation of STAT3 might have significance. We conclude that NLGP may be effective in maintaining normal immune homeostasis by upregulating type 1 response in immunosuppressed hosts, which may have significant role in the induction of host protective antitumor functions.</description><identifier>ISSN: 0198-8859</identifier><identifier>EISSN: 1879-1166</identifier><identifier>DOI: 10.1016/j.humimm.2008.09.004</identifier><identifier>PMID: 18983881</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>Adult ; Allergy and Immunology ; Animals ; Antigens, CD - immunology ; Antigens, Differentiation, T-Lymphocyte - immunology ; Azadirachta - chemistry ; Cells, Cultured ; Cytokines - biosynthesis ; Dendritic Cells - drug effects ; Dendritic Cells - immunology ; Female ; Glycoproteins - pharmacology ; Humans ; Interferon-gamma - biosynthesis ; L-Selectin - immunology ; Lectins, C-Type ; Leukocyte Common Antigens - immunology ; Lymphocytes - drug effects ; Lymphocytes - immunology ; Mice ; Middle Aged ; Monocytes - drug effects ; Monocytes - immunology ; Neem leaf glycoprotein ; Phosphorylation ; Plant Leaves - chemistry ; STAT Transcription Factors - metabolism ; T-bet ; T-Box Domain Proteins - immunology ; Type 1 immune response ; Young Adult</subject><ispartof>Human immunology, 2009, Vol.70 (1), p.6-15</ispartof><rights>American Society for Histocompatibility and Immunogenetics</rights><rights>2009 American Society for Histocompatibility and Immunogenetics</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c446t-82db4d43b8d83320a73cce92dcfd5e3a461bb8c34d622abe3d671bd5797111843</citedby><cites>FETCH-LOGICAL-c446t-82db4d43b8d83320a73cce92dcfd5e3a461bb8c34d622abe3d671bd5797111843</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,4024,27923,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/18983881$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Bose, Anamika</creatorcontrib><creatorcontrib>Chakraborty, Krishnendu</creatorcontrib><creatorcontrib>Sarkar, Koustav</creatorcontrib><creatorcontrib>Goswami, Shyamal</creatorcontrib><creatorcontrib>Haque, Enamul</creatorcontrib><creatorcontrib>Chakraborty, Tathagata</creatorcontrib><creatorcontrib>Ghosh, Diptendu</creatorcontrib><creatorcontrib>Roy, Soumyabrata</creatorcontrib><creatorcontrib>Laskar, Subrata</creatorcontrib><creatorcontrib>Baral, Rathindranath</creatorcontrib><title>Neem leaf glycoprotein directs T-bet–associated type 1 immune commitment</title><title>Human immunology</title><addtitle>Hum Immunol</addtitle><description>Abstract Neem leaf glycoprotein (NLGP)–mediated immune activation and associated immune polarization was studied. NLGP–induced activation is reflected in upregulation of early activation marker CD69 on lymphocytes, monocytes, and dendritic cells. Activation is also denoted by CD45RO enhancement, with a decrease in CD45RA phenotype and CD62L (L-selectin). NLGP-activated T cells secrete greater amount of signature T-helper (Th)1 cytokines interferon-γ and a lower amount of the Th2 cytokine interleukin (IL)–4. Similar type 1 directiveness is also observed in antigen-presenting monocytes and dendritic cells by upregulation of IL-12, tumor necrosis factor –α and downregulation of IL-10. Creation of the type 1 microenvironment is also assisted by NLGP-induced downregulation of FoxP3+ T-Reg cells. A type 1–specific transcription factor, T-bet, is upregulated in circulating immune cells after their stimulation with NLGP. In the creation of type 1 immune network, increased phosphorylation of STAT1 and STAT4 with decreased phosphorylation of STAT3 might have significance. We conclude that NLGP may be effective in maintaining normal immune homeostasis by upregulating type 1 response in immunosuppressed hosts, which may have significant role in the induction of host protective antitumor functions.</description><subject>Adult</subject><subject>Allergy and Immunology</subject><subject>Animals</subject><subject>Antigens, CD - immunology</subject><subject>Antigens, Differentiation, T-Lymphocyte - immunology</subject><subject>Azadirachta - chemistry</subject><subject>Cells, Cultured</subject><subject>Cytokines - biosynthesis</subject><subject>Dendritic Cells - drug effects</subject><subject>Dendritic Cells - immunology</subject><subject>Female</subject><subject>Glycoproteins - pharmacology</subject><subject>Humans</subject><subject>Interferon-gamma - biosynthesis</subject><subject>L-Selectin - immunology</subject><subject>Lectins, C-Type</subject><subject>Leukocyte Common Antigens - immunology</subject><subject>Lymphocytes - drug effects</subject><subject>Lymphocytes - immunology</subject><subject>Mice</subject><subject>Middle Aged</subject><subject>Monocytes - drug effects</subject><subject>Monocytes - immunology</subject><subject>Neem leaf glycoprotein</subject><subject>Phosphorylation</subject><subject>Plant Leaves - chemistry</subject><subject>STAT Transcription Factors - metabolism</subject><subject>T-bet</subject><subject>T-Box Domain Proteins - immunology</subject><subject>Type 1 immune response</subject><subject>Young Adult</subject><issn>0198-8859</issn><issn>1879-1166</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2009</creationdate><recordtype>article</recordtype><recordid>eNqFkcuO1DAQRS0EYnoG_gChrNgllB_txwYJjXgMGsGCYW05djW4iZMmdpB6xz_wh3wJbqUlJDazqs25t0qnCHlGoaNA5ct9921JMaWOAegOTAcgHpAN1cq0lEr5kGyAGt1qvTUX5DLnPQAoUOIxuaDaaK413ZAPHxFTM6DbNV-Ho58O81Qwjk2IM_qSm7u2x_Ln12-X8-SjKxiacjxgQ5u6ehmx8VNKsSQcyxPyaOeGjE_P84p8efvm7vp9e_vp3c3169vWCyFLq1noRRC810FzzsAp7j0aFvwubJE7IWnfa89FkIy5HnmQivZhq4yilGrBr8iLtbfe-mPBXGyK2eMwuBGnJVsplTFGb-8FGTDBldIVFCvo5ynnGXf2MMfk5qOlYE-y7d6usu1JtgVjq-wae37uX_qE4V_obLcCr1YAq46fEWebfcTR42rXhinet-H_Aj_EMXo3fMcj5v20zGNVbanNzIL9fHr46d-ga1oJyf8CjLCoNA</recordid><startdate>2009</startdate><enddate>2009</enddate><creator>Bose, Anamika</creator><creator>Chakraborty, Krishnendu</creator><creator>Sarkar, Koustav</creator><creator>Goswami, Shyamal</creator><creator>Haque, Enamul</creator><creator>Chakraborty, Tathagata</creator><creator>Ghosh, Diptendu</creator><creator>Roy, Soumyabrata</creator><creator>Laskar, Subrata</creator><creator>Baral, Rathindranath</creator><general>Elsevier Inc</general><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>2009</creationdate><title>Neem leaf glycoprotein directs T-bet–associated type 1 immune commitment</title><author>Bose, Anamika ; Chakraborty, Krishnendu ; Sarkar, Koustav ; Goswami, Shyamal ; Haque, Enamul ; Chakraborty, Tathagata ; Ghosh, Diptendu ; Roy, Soumyabrata ; Laskar, Subrata ; Baral, Rathindranath</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c446t-82db4d43b8d83320a73cce92dcfd5e3a461bb8c34d622abe3d671bd5797111843</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2009</creationdate><topic>Adult</topic><topic>Allergy and Immunology</topic><topic>Animals</topic><topic>Antigens, CD - immunology</topic><topic>Antigens, Differentiation, T-Lymphocyte - immunology</topic><topic>Azadirachta - chemistry</topic><topic>Cells, Cultured</topic><topic>Cytokines - biosynthesis</topic><topic>Dendritic Cells - drug effects</topic><topic>Dendritic Cells - immunology</topic><topic>Female</topic><topic>Glycoproteins - pharmacology</topic><topic>Humans</topic><topic>Interferon-gamma - biosynthesis</topic><topic>L-Selectin - immunology</topic><topic>Lectins, C-Type</topic><topic>Leukocyte Common Antigens - immunology</topic><topic>Lymphocytes - drug effects</topic><topic>Lymphocytes - immunology</topic><topic>Mice</topic><topic>Middle Aged</topic><topic>Monocytes - drug effects</topic><topic>Monocytes - immunology</topic><topic>Neem leaf glycoprotein</topic><topic>Phosphorylation</topic><topic>Plant Leaves - chemistry</topic><topic>STAT Transcription Factors - metabolism</topic><topic>T-bet</topic><topic>T-Box Domain Proteins - immunology</topic><topic>Type 1 immune response</topic><topic>Young Adult</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Bose, Anamika</creatorcontrib><creatorcontrib>Chakraborty, Krishnendu</creatorcontrib><creatorcontrib>Sarkar, Koustav</creatorcontrib><creatorcontrib>Goswami, Shyamal</creatorcontrib><creatorcontrib>Haque, Enamul</creatorcontrib><creatorcontrib>Chakraborty, Tathagata</creatorcontrib><creatorcontrib>Ghosh, Diptendu</creatorcontrib><creatorcontrib>Roy, Soumyabrata</creatorcontrib><creatorcontrib>Laskar, Subrata</creatorcontrib><creatorcontrib>Baral, Rathindranath</creatorcontrib><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>Human immunology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Bose, Anamika</au><au>Chakraborty, Krishnendu</au><au>Sarkar, Koustav</au><au>Goswami, Shyamal</au><au>Haque, Enamul</au><au>Chakraborty, Tathagata</au><au>Ghosh, Diptendu</au><au>Roy, Soumyabrata</au><au>Laskar, Subrata</au><au>Baral, Rathindranath</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Neem leaf glycoprotein directs T-bet–associated type 1 immune commitment</atitle><jtitle>Human immunology</jtitle><addtitle>Hum Immunol</addtitle><date>2009</date><risdate>2009</risdate><volume>70</volume><issue>1</issue><spage>6</spage><epage>15</epage><pages>6-15</pages><issn>0198-8859</issn><eissn>1879-1166</eissn><abstract>Abstract Neem leaf glycoprotein (NLGP)–mediated immune activation and associated immune polarization was studied. NLGP–induced activation is reflected in upregulation of early activation marker CD69 on lymphocytes, monocytes, and dendritic cells. Activation is also denoted by CD45RO enhancement, with a decrease in CD45RA phenotype and CD62L (L-selectin). NLGP-activated T cells secrete greater amount of signature T-helper (Th)1 cytokines interferon-γ and a lower amount of the Th2 cytokine interleukin (IL)–4. Similar type 1 directiveness is also observed in antigen-presenting monocytes and dendritic cells by upregulation of IL-12, tumor necrosis factor –α and downregulation of IL-10. Creation of the type 1 microenvironment is also assisted by NLGP-induced downregulation of FoxP3+ T-Reg cells. A type 1–specific transcription factor, T-bet, is upregulated in circulating immune cells after their stimulation with NLGP. In the creation of type 1 immune network, increased phosphorylation of STAT1 and STAT4 with decreased phosphorylation of STAT3 might have significance. We conclude that NLGP may be effective in maintaining normal immune homeostasis by upregulating type 1 response in immunosuppressed hosts, which may have significant role in the induction of host protective antitumor functions.</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>18983881</pmid><doi>10.1016/j.humimm.2008.09.004</doi><tpages>10</tpages></addata></record> |
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subjects | Adult Allergy and Immunology Animals Antigens, CD - immunology Antigens, Differentiation, T-Lymphocyte - immunology Azadirachta - chemistry Cells, Cultured Cytokines - biosynthesis Dendritic Cells - drug effects Dendritic Cells - immunology Female Glycoproteins - pharmacology Humans Interferon-gamma - biosynthesis L-Selectin - immunology Lectins, C-Type Leukocyte Common Antigens - immunology Lymphocytes - drug effects Lymphocytes - immunology Mice Middle Aged Monocytes - drug effects Monocytes - immunology Neem leaf glycoprotein Phosphorylation Plant Leaves - chemistry STAT Transcription Factors - metabolism T-bet T-Box Domain Proteins - immunology Type 1 immune response Young Adult |
title | Neem leaf glycoprotein directs T-bet–associated type 1 immune commitment |
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