Th1/Th2 cells in inflammatory disease states: therapeutic implications
Inflammation is initiated as a protective response by the host, but can often result in systemic pathology. Among cells of the immune system, T lympho-cytes play a major role in the inflammatory response. T cell inflammation is characterised histologically by an infiltration of mononuclear cells. Ke...
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Veröffentlicht in: | Expert opinion on biological therapy 2004-12, Vol.4 (12), p.1887-1896 |
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container_end_page | 1896 |
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container_issue | 12 |
container_start_page | 1887 |
container_title | Expert opinion on biological therapy |
container_volume | 4 |
creator | Moss, Ronald B Moll, Thomas El-Kalay, Mohammad Kohne, Connie Soo Hoo, William Encinas, Jeffrey Carlo, Dennis J |
description | Inflammation is initiated as a protective response by the host, but can often result in systemic pathology. Among cells of the immune system, T lympho-cytes play a major role in the inflammatory response. T cell inflammation is characterised histologically by an infiltration of mononuclear cells. Key regulators of this response are a subset of T lymphocytes called T helper (Th) cells. These cells secrete soluble mediators called cytokines, which orchestrate the immune response. The appropriate regulation of Th cell immunity is critical in the control and prevention of diverse disease states. This review will focus on the role of Th cells in the inflammatory process involved in allergic disease, diabetes, infectious disease, rheumatoid arthritis, heart disease, multiple sclerosis and cancer. In the area of autoimmunity, in particular, a basic understanding of Th cells and cytokines has contributed to the development of clinically efficacious biological agents. This review also examines current and novel treatment strategies under investigation at present that regulate Th cell immunity, which may result in better treatments for immune-mediated diseases. |
doi_str_mv | 10.1517/14712598.4.12.1887 |
format | Article |
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Among cells of the immune system, T lympho-cytes play a major role in the inflammatory response. T cell inflammation is characterised histologically by an infiltration of mononuclear cells. Key regulators of this response are a subset of T lymphocytes called T helper (Th) cells. These cells secrete soluble mediators called cytokines, which orchestrate the immune response. The appropriate regulation of Th cell immunity is critical in the control and prevention of diverse disease states. This review will focus on the role of Th cells in the inflammatory process involved in allergic disease, diabetes, infectious disease, rheumatoid arthritis, heart disease, multiple sclerosis and cancer. In the area of autoimmunity, in particular, a basic understanding of Th cells and cytokines has contributed to the development of clinically efficacious biological agents. This review also examines current and novel treatment strategies under investigation at present that regulate Th cell immunity, which may result in better treatments for immune-mediated diseases.</description><subject>allergy</subject><subject>Animals</subject><subject>Anti-Inflammatory Agents - immunology</subject><subject>Anti-Inflammatory Agents - therapeutic use</subject><subject>Autoimmune Diseases - drug therapy</subject><subject>Autoimmune Diseases - immunology</subject><subject>autoimmunity</subject><subject>cancer</subject><subject>CpG</subject><subject>heat-shock proteins</subject><subject>Histocompatibility Antigens Class II - immunology</subject><subject>Humans</subject><subject>infectious disease</subject><subject>inflammation</subject><subject>Inflammation - drug therapy</subject><subject>Inflammation - immunology</subject><subject>T cell immunoglobulin mucin domain</subject><subject>T helper</subject><subject>Th1 Cells - immunology</subject><subject>Th2 Cells - immunology</subject><subject>TIM-1</subject><subject>TIM-3</subject><issn>1471-2598</issn><issn>1744-7682</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2004</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkM2KFDEUhYMozo--gAuplbvqqZufSiK6kMEZhQE37TrcSidUhqpKm6SQfvtJ0y3iZoRAsvjOzbkfIe-g24AAeQNcAhVabfgG6AaUki_IJUjOW9kr-rK-K9AeiQtylfNj19FOC_qaXIAQEriAS3K3HeFmO9LGumnKTVjq8RPOM5aYDs0uZIfZNblgcfljU0aXcO_WEmwT5v0ULJYQl_yGvPI4Zff2fF-Tn3dft7ff2ocf999vvzy0ljNdWga9072tjRwy4VU_wOBRD0pYRE2V7wepBqjdrFZa6IFJxjXtqAXmB0_ZNflwmrtP8dfqcjFzyMfquLi4ZtNLYLIu-V-QdqyTvGcVpCfQpphzct7sU5gxHQx05qjZ_NFsuAFqjppr6P15-jrMbvc3cvZagc8noNqMacbfMU07U_AwxeQTLjZkw5794NM_-dHhVEaLyZnHuKalOn6u3xNHqp47</recordid><startdate>20041201</startdate><enddate>20041201</enddate><creator>Moss, Ronald B</creator><creator>Moll, Thomas</creator><creator>El-Kalay, Mohammad</creator><creator>Kohne, Connie</creator><creator>Soo Hoo, William</creator><creator>Encinas, Jeffrey</creator><creator>Carlo, Dennis J</creator><general>Ashley Publications Ltd</general><general>Taylor & Francis</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>20041201</creationdate><title>Th1/Th2 cells in inflammatory disease states: therapeutic implications</title><author>Moss, Ronald B ; Moll, Thomas ; El-Kalay, Mohammad ; Kohne, Connie ; Soo Hoo, William ; Encinas, Jeffrey ; Carlo, Dennis J</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c439t-316e96c598ea35f86b1bfa9b85caa928f6b78b1714c98959b37349202c13fbf23</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2004</creationdate><topic>allergy</topic><topic>Animals</topic><topic>Anti-Inflammatory Agents - immunology</topic><topic>Anti-Inflammatory Agents - therapeutic use</topic><topic>Autoimmune Diseases - drug therapy</topic><topic>Autoimmune Diseases - immunology</topic><topic>autoimmunity</topic><topic>cancer</topic><topic>CpG</topic><topic>heat-shock proteins</topic><topic>Histocompatibility Antigens Class II - immunology</topic><topic>Humans</topic><topic>infectious disease</topic><topic>inflammation</topic><topic>Inflammation - drug therapy</topic><topic>Inflammation - immunology</topic><topic>T cell immunoglobulin mucin domain</topic><topic>T helper</topic><topic>Th1 Cells - immunology</topic><topic>Th2 Cells - immunology</topic><topic>TIM-1</topic><topic>TIM-3</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Moss, Ronald B</creatorcontrib><creatorcontrib>Moll, Thomas</creatorcontrib><creatorcontrib>El-Kalay, Mohammad</creatorcontrib><creatorcontrib>Kohne, Connie</creatorcontrib><creatorcontrib>Soo Hoo, William</creatorcontrib><creatorcontrib>Encinas, Jeffrey</creatorcontrib><creatorcontrib>Carlo, Dennis J</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>Expert opinion on biological therapy</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Moss, Ronald B</au><au>Moll, Thomas</au><au>El-Kalay, Mohammad</au><au>Kohne, Connie</au><au>Soo Hoo, William</au><au>Encinas, Jeffrey</au><au>Carlo, Dennis J</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Th1/Th2 cells in inflammatory disease states: therapeutic implications</atitle><jtitle>Expert opinion on biological therapy</jtitle><addtitle>Expert Opin Biol Ther</addtitle><date>2004-12-01</date><risdate>2004</risdate><volume>4</volume><issue>12</issue><spage>1887</spage><epage>1896</epage><pages>1887-1896</pages><issn>1471-2598</issn><eissn>1744-7682</eissn><abstract>Inflammation is initiated as a protective response by the host, but can often result in systemic pathology. Among cells of the immune system, T lympho-cytes play a major role in the inflammatory response. T cell inflammation is characterised histologically by an infiltration of mononuclear cells. Key regulators of this response are a subset of T lymphocytes called T helper (Th) cells. These cells secrete soluble mediators called cytokines, which orchestrate the immune response. The appropriate regulation of Th cell immunity is critical in the control and prevention of diverse disease states. This review will focus on the role of Th cells in the inflammatory process involved in allergic disease, diabetes, infectious disease, rheumatoid arthritis, heart disease, multiple sclerosis and cancer. In the area of autoimmunity, in particular, a basic understanding of Th cells and cytokines has contributed to the development of clinically efficacious biological agents. This review also examines current and novel treatment strategies under investigation at present that regulate Th cell immunity, which may result in better treatments for immune-mediated diseases.</abstract><cop>England</cop><pub>Ashley Publications Ltd</pub><pmid>15571451</pmid><doi>10.1517/14712598.4.12.1887</doi><tpages>10</tpages></addata></record> |
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subjects | allergy Animals Anti-Inflammatory Agents - immunology Anti-Inflammatory Agents - therapeutic use Autoimmune Diseases - drug therapy Autoimmune Diseases - immunology autoimmunity cancer CpG heat-shock proteins Histocompatibility Antigens Class II - immunology Humans infectious disease inflammation Inflammation - drug therapy Inflammation - immunology T cell immunoglobulin mucin domain T helper Th1 Cells - immunology Th2 Cells - immunology TIM-1 TIM-3 |
title | Th1/Th2 cells in inflammatory disease states: therapeutic implications |
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