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Immunological characteristics and effect of cyclosporin in patients with immune thrombocytopenia
Objective Immune thrombocytopenia (ITP) is well‐known as an antibody‐mediated autoimmune disease, and it is easy to get response but often turns to relapse or refractory. Cyclosporin is a traditional immunosuppressant and had a good effect on ITP patients. In this paper, we retrospectively analyze t...
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Published in: | Journal of clinical laboratory analysis 2021-09, Vol.35 (9), p.e23922-n/a |
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creator | Wang, Ting He, Xin Ran, Ningyuan Liu, Chunyan Xing, Limin Wang, Huaquan Fu, Rong Shao, Zonghong |
description | Objective
Immune thrombocytopenia (ITP) is well‐known as an antibody‐mediated autoimmune disease, and it is easy to get response but often turns to relapse or refractory. Cyclosporin is a traditional immunosuppressant and had a good effect on ITP patients. In this paper, we retrospectively analyze the immunological characteristics and therapeutic effect of cyclosporin in 220 patients with ITP.
Methods
All newly diagnosed ITP patients in the Department of Hematology, Tianjin Medical University General Hospital from June 2018 to December 2020 were enrolled and divided into four groups according to the expression of autoantibodies and the occurrence of prodromal infection. The basic data and immune indexes of ITP patients in each group were collected. The clinical immunological characteristics of patients in each group and the therapeutic effect of cyclosporin in each group were analyzed.
Results
Multi‐autoantibody ITP patients were more likely to have low serum albumin and high gamma globulin, and the ratio of albumin to globulin decreased. In addition, the level of IgA and IgG increased and the level of complement C3 and C4 decreased more frequently than those in other groups. The number of CD3+T lymphocytes, especially CD3+CD4+T lymphocytes, decreased in ANA+ITP patients. The number of CD16+CD56+NK cells, pDC/DC ratio, and pDC/mDC ratio were higher than those in other groups. The expression of IL‐6 and the proportion of CD19+B lymphocytes increased in two groups of ITP patients with abnormal autoantibodies. The patients of pro‐infected group were more likely to suffer from coagulation disorder. After treatment with cyclosporin, the response rate increased and the 3‐month relapse rate decreased in all ITP patients, and the therapeutic effect of patients with high megakaryocyte number was significantly higher than that of patients with low megakaryocyte number. The impact factors that influence the effect of glucocorticoid and(or) IVIG were the number of CD3+CD8+T lymphocytes, CD4/CD8 cell ratio, and the number of CD19+B lymphocytes. The independent impact factor of cyclosporin therapeutic response rate was the number of CD3+T lymphocytes.
Conclusions
ITP is a heterogeneous disease, recurrence may occur during or rapidly after treatment.
Cyclosporine included treatment can improve the effective rate of ITP and
reduce the relapse rate within 3 months. The number of CD3+T lymphocytes was
the only impact factor that influence the therapeutic effect of
cyclospor |
doi_str_mv | 10.1002/jcla.23922 |
format | article |
fullrecord | <record><control><sourceid>proquest_pubme</sourceid><recordid>TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_8418498</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>2557231847</sourcerecordid><originalsourceid>FETCH-LOGICAL-c4482-c8193f8ff350cdc9c83d56ef1a70d301abf67ba752dbaaca91bec8e6bbf3c3b53</originalsourceid><addsrcrecordid>eNp9kU1r3DAQhkVpaDZpL_0BRdBLCTjVh2XLl0JY-pGykEt7VqWxlNViW64kN-y_rzabhraHwMAc5uHhHV6EXlNySQlh73cw6EvGO8aeoRUlnayYZOI5WhEp20oSyk_RWUo7QojsaPMCnfKas07QZoV-XI_jMoUh3HrQA4atjhqyjT5lDwnrqcfWOQsZB4dhD0NIc4h-wmVmnb2dcsJ3Pm-xP4gsztsYRhNgn8NsJ69fohOnh2RfPexz9P3Tx2_rL9Xm5vP1-mpTQV1LVoGkHXfSOS4I9NCB5L1orKO6JT0nVBvXtEa3gvVGa9AdNRakbYxxHLgR_Bx9OHrnxYy2hxIs6kHN0Y867lXQXv17mfxW3YZfStZU1p0sgncPghh-LjZlNfoEdhj0ZMOSFBOiZbywbUHf_ofuwhKn8l6hmo5IKgUr1MWRghhSitY9hqFEHYpTh-LUfXEFfvN3_Ef0T1MFoEfgzg92_4RKfV1vro7S397Vp0M</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2569081852</pqid></control><display><type>article</type><title>Immunological characteristics and effect of cyclosporin in patients with immune thrombocytopenia</title><source>Wiley-Blackwell Open Access Collection</source><source>Open Access: PubMed Central</source><source>Publicly Available Content Database</source><creator>Wang, Ting ; He, Xin ; Ran, Ningyuan ; Liu, Chunyan ; Xing, Limin ; Wang, Huaquan ; Fu, Rong ; Shao, Zonghong</creator><creatorcontrib>Wang, Ting ; He, Xin ; Ran, Ningyuan ; Liu, Chunyan ; Xing, Limin ; Wang, Huaquan ; Fu, Rong ; Shao, Zonghong</creatorcontrib><description>Objective
Immune thrombocytopenia (ITP) is well‐known as an antibody‐mediated autoimmune disease, and it is easy to get response but often turns to relapse or refractory. Cyclosporin is a traditional immunosuppressant and had a good effect on ITP patients. In this paper, we retrospectively analyze the immunological characteristics and therapeutic effect of cyclosporin in 220 patients with ITP.
Methods
All newly diagnosed ITP patients in the Department of Hematology, Tianjin Medical University General Hospital from June 2018 to December 2020 were enrolled and divided into four groups according to the expression of autoantibodies and the occurrence of prodromal infection. The basic data and immune indexes of ITP patients in each group were collected. The clinical immunological characteristics of patients in each group and the therapeutic effect of cyclosporin in each group were analyzed.
Results
Multi‐autoantibody ITP patients were more likely to have low serum albumin and high gamma globulin, and the ratio of albumin to globulin decreased. In addition, the level of IgA and IgG increased and the level of complement C3 and C4 decreased more frequently than those in other groups. The number of CD3+T lymphocytes, especially CD3+CD4+T lymphocytes, decreased in ANA+ITP patients. The number of CD16+CD56+NK cells, pDC/DC ratio, and pDC/mDC ratio were higher than those in other groups. The expression of IL‐6 and the proportion of CD19+B lymphocytes increased in two groups of ITP patients with abnormal autoantibodies. The patients of pro‐infected group were more likely to suffer from coagulation disorder. After treatment with cyclosporin, the response rate increased and the 3‐month relapse rate decreased in all ITP patients, and the therapeutic effect of patients with high megakaryocyte number was significantly higher than that of patients with low megakaryocyte number. The impact factors that influence the effect of glucocorticoid and(or) IVIG were the number of CD3+CD8+T lymphocytes, CD4/CD8 cell ratio, and the number of CD19+B lymphocytes. The independent impact factor of cyclosporin therapeutic response rate was the number of CD3+T lymphocytes.
Conclusions
ITP is a heterogeneous disease, recurrence may occur during or rapidly after treatment.
Cyclosporine included treatment can improve the effective rate of ITP and
reduce the relapse rate within 3 months. The number of CD3+T lymphocytes was
the only impact factor that influence the therapeutic effect of
cyclosporin in ITP patients.
We showed clinical characteristics of four subgroups of ITP patients according to immune indexes and proinfection. The patients with autoantibodies usually combined with imbalance of immune cells. Comparing with glucocorticoid and(or) IVIG only treatment, cyclosporin‐included regimen has a higher response rate and lower relapse rate. The number of CD3+T lymphocytes is the independent impact factor that influence the therapeutic effect of cyclosporin.</description><identifier>ISSN: 0887-8013</identifier><identifier>EISSN: 1098-2825</identifier><identifier>DOI: 10.1002/jcla.23922</identifier><identifier>PMID: 34329516</identifier><language>eng</language><publisher>United States: John Wiley & Sons, Inc</publisher><subject>Adult ; Aged ; Aged, 80 and over ; Albumin ; Antibodies ; antinuclear antibodies ; Autoantibodies ; Autoimmune diseases ; B-Lymphocytes - immunology ; Blood platelets ; CD16 antigen ; CD19 antigen ; CD3 antigen ; CD3+T lymphocytes ; CD4 antigen ; CD56 antigen ; CD8 antigen ; CD8-Positive T-Lymphocytes - immunology ; Complement component C3 ; Complement component C4 ; cyclosporin ; Cyclosporine - therapeutic use ; Cyclosporins ; Cytokines ; Drug dosages ; Drug therapy ; Female ; Females ; Flow cytometry ; Follow-Up Studies ; Globulins ; Glucocorticoids ; Hematology ; Hemorrhage ; Hospitals ; Humans ; Idiopathic thrombocytopenic purpura ; immune cell subsets ; immune thrombocytopenia ; Immunoglobulin A ; Immunoglobulin G ; Immunology ; Immunosuppressive Agents - therapeutic use ; Infections ; Intravenous administration ; Killer Cells, Natural - immunology ; Lymphocytes ; Lymphocytes B ; Lymphocytes T ; Male ; Medical laboratories ; Middle Aged ; Patients ; Prognosis ; Purpura, Thrombocytopenic, Idiopathic - drug therapy ; Purpura, Thrombocytopenic, Idiopathic - immunology ; Purpura, Thrombocytopenic, Idiopathic - pathology ; Retrospective Studies ; Thrombocytopenia</subject><ispartof>Journal of clinical laboratory analysis, 2021-09, Vol.35 (9), p.e23922-n/a</ispartof><rights>2021 The Authors. published by Wiley Periodicals LLC.</rights><rights>2021 The Authors. Journal of Clinical Laboratory Analysis published by Wiley Periodicals LLC.</rights><rights>2021. This work is published under http://creativecommons.org/licenses/by-nc-nd/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4482-c8193f8ff350cdc9c83d56ef1a70d301abf67ba752dbaaca91bec8e6bbf3c3b53</citedby><cites>FETCH-LOGICAL-c4482-c8193f8ff350cdc9c83d56ef1a70d301abf67ba752dbaaca91bec8e6bbf3c3b53</cites><orcidid>0000-0002-9928-9224</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.proquest.com/docview/2569081852/fulltextPDF?pq-origsite=primo$$EPDF$$P50$$Gproquest$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/2569081852?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>230,314,723,776,780,881,11541,25731,27901,27902,36989,36990,44566,46027,46451,53766,53768,74869</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/34329516$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Wang, Ting</creatorcontrib><creatorcontrib>He, Xin</creatorcontrib><creatorcontrib>Ran, Ningyuan</creatorcontrib><creatorcontrib>Liu, Chunyan</creatorcontrib><creatorcontrib>Xing, Limin</creatorcontrib><creatorcontrib>Wang, Huaquan</creatorcontrib><creatorcontrib>Fu, Rong</creatorcontrib><creatorcontrib>Shao, Zonghong</creatorcontrib><title>Immunological characteristics and effect of cyclosporin in patients with immune thrombocytopenia</title><title>Journal of clinical laboratory analysis</title><addtitle>J Clin Lab Anal</addtitle><description>Objective
Immune thrombocytopenia (ITP) is well‐known as an antibody‐mediated autoimmune disease, and it is easy to get response but often turns to relapse or refractory. Cyclosporin is a traditional immunosuppressant and had a good effect on ITP patients. In this paper, we retrospectively analyze the immunological characteristics and therapeutic effect of cyclosporin in 220 patients with ITP.
Methods
All newly diagnosed ITP patients in the Department of Hematology, Tianjin Medical University General Hospital from June 2018 to December 2020 were enrolled and divided into four groups according to the expression of autoantibodies and the occurrence of prodromal infection. The basic data and immune indexes of ITP patients in each group were collected. The clinical immunological characteristics of patients in each group and the therapeutic effect of cyclosporin in each group were analyzed.
Results
Multi‐autoantibody ITP patients were more likely to have low serum albumin and high gamma globulin, and the ratio of albumin to globulin decreased. In addition, the level of IgA and IgG increased and the level of complement C3 and C4 decreased more frequently than those in other groups. The number of CD3+T lymphocytes, especially CD3+CD4+T lymphocytes, decreased in ANA+ITP patients. The number of CD16+CD56+NK cells, pDC/DC ratio, and pDC/mDC ratio were higher than those in other groups. The expression of IL‐6 and the proportion of CD19+B lymphocytes increased in two groups of ITP patients with abnormal autoantibodies. The patients of pro‐infected group were more likely to suffer from coagulation disorder. After treatment with cyclosporin, the response rate increased and the 3‐month relapse rate decreased in all ITP patients, and the therapeutic effect of patients with high megakaryocyte number was significantly higher than that of patients with low megakaryocyte number. The impact factors that influence the effect of glucocorticoid and(or) IVIG were the number of CD3+CD8+T lymphocytes, CD4/CD8 cell ratio, and the number of CD19+B lymphocytes. The independent impact factor of cyclosporin therapeutic response rate was the number of CD3+T lymphocytes.
Conclusions
ITP is a heterogeneous disease, recurrence may occur during or rapidly after treatment.
Cyclosporine included treatment can improve the effective rate of ITP and
reduce the relapse rate within 3 months. The number of CD3+T lymphocytes was
the only impact factor that influence the therapeutic effect of
cyclosporin in ITP patients.
We showed clinical characteristics of four subgroups of ITP patients according to immune indexes and proinfection. The patients with autoantibodies usually combined with imbalance of immune cells. Comparing with glucocorticoid and(or) IVIG only treatment, cyclosporin‐included regimen has a higher response rate and lower relapse rate. The number of CD3+T lymphocytes is the independent impact factor that influence the therapeutic effect of cyclosporin.</description><subject>Adult</subject><subject>Aged</subject><subject>Aged, 80 and over</subject><subject>Albumin</subject><subject>Antibodies</subject><subject>antinuclear antibodies</subject><subject>Autoantibodies</subject><subject>Autoimmune diseases</subject><subject>B-Lymphocytes - immunology</subject><subject>Blood platelets</subject><subject>CD16 antigen</subject><subject>CD19 antigen</subject><subject>CD3 antigen</subject><subject>CD3+T lymphocytes</subject><subject>CD4 antigen</subject><subject>CD56 antigen</subject><subject>CD8 antigen</subject><subject>CD8-Positive T-Lymphocytes - immunology</subject><subject>Complement component C3</subject><subject>Complement component C4</subject><subject>cyclosporin</subject><subject>Cyclosporine - therapeutic use</subject><subject>Cyclosporins</subject><subject>Cytokines</subject><subject>Drug dosages</subject><subject>Drug therapy</subject><subject>Female</subject><subject>Females</subject><subject>Flow cytometry</subject><subject>Follow-Up Studies</subject><subject>Globulins</subject><subject>Glucocorticoids</subject><subject>Hematology</subject><subject>Hemorrhage</subject><subject>Hospitals</subject><subject>Humans</subject><subject>Idiopathic thrombocytopenic purpura</subject><subject>immune cell subsets</subject><subject>immune thrombocytopenia</subject><subject>Immunoglobulin A</subject><subject>Immunoglobulin G</subject><subject>Immunology</subject><subject>Immunosuppressive Agents - therapeutic use</subject><subject>Infections</subject><subject>Intravenous administration</subject><subject>Killer Cells, Natural - immunology</subject><subject>Lymphocytes</subject><subject>Lymphocytes B</subject><subject>Lymphocytes T</subject><subject>Male</subject><subject>Medical laboratories</subject><subject>Middle Aged</subject><subject>Patients</subject><subject>Prognosis</subject><subject>Purpura, Thrombocytopenic, Idiopathic - drug therapy</subject><subject>Purpura, Thrombocytopenic, Idiopathic - immunology</subject><subject>Purpura, Thrombocytopenic, Idiopathic - pathology</subject><subject>Retrospective Studies</subject><subject>Thrombocytopenia</subject><issn>0887-8013</issn><issn>1098-2825</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2021</creationdate><recordtype>article</recordtype><sourceid>24P</sourceid><sourceid>PIMPY</sourceid><recordid>eNp9kU1r3DAQhkVpaDZpL_0BRdBLCTjVh2XLl0JY-pGykEt7VqWxlNViW64kN-y_rzabhraHwMAc5uHhHV6EXlNySQlh73cw6EvGO8aeoRUlnayYZOI5WhEp20oSyk_RWUo7QojsaPMCnfKas07QZoV-XI_jMoUh3HrQA4atjhqyjT5lDwnrqcfWOQsZB4dhD0NIc4h-wmVmnb2dcsJ3Pm-xP4gsztsYRhNgn8NsJ69fohOnh2RfPexz9P3Tx2_rL9Xm5vP1-mpTQV1LVoGkHXfSOS4I9NCB5L1orKO6JT0nVBvXtEa3gvVGa9AdNRakbYxxHLgR_Bx9OHrnxYy2hxIs6kHN0Y867lXQXv17mfxW3YZfStZU1p0sgncPghh-LjZlNfoEdhj0ZMOSFBOiZbywbUHf_ofuwhKn8l6hmo5IKgUr1MWRghhSitY9hqFEHYpTh-LUfXEFfvN3_Ef0T1MFoEfgzg92_4RKfV1vro7S397Vp0M</recordid><startdate>202109</startdate><enddate>202109</enddate><creator>Wang, Ting</creator><creator>He, Xin</creator><creator>Ran, Ningyuan</creator><creator>Liu, Chunyan</creator><creator>Xing, Limin</creator><creator>Wang, Huaquan</creator><creator>Fu, Rong</creator><creator>Shao, Zonghong</creator><general>John Wiley & Sons, Inc</general><general>John Wiley and Sons Inc</general><scope>24P</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>3V.</scope><scope>7QP</scope><scope>7T5</scope><scope>7U9</scope><scope>7X7</scope><scope>7XB</scope><scope>8C1</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>H94</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>LK8</scope><scope>M0S</scope><scope>M7P</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7X8</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0002-9928-9224</orcidid></search><sort><creationdate>202109</creationdate><title>Immunological characteristics and effect of cyclosporin in patients with immune thrombocytopenia</title><author>Wang, Ting ; He, Xin ; Ran, Ningyuan ; Liu, Chunyan ; Xing, Limin ; Wang, Huaquan ; Fu, Rong ; Shao, Zonghong</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4482-c8193f8ff350cdc9c83d56ef1a70d301abf67ba752dbaaca91bec8e6bbf3c3b53</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2021</creationdate><topic>Adult</topic><topic>Aged</topic><topic>Aged, 80 and over</topic><topic>Albumin</topic><topic>Antibodies</topic><topic>antinuclear antibodies</topic><topic>Autoantibodies</topic><topic>Autoimmune diseases</topic><topic>B-Lymphocytes - immunology</topic><topic>Blood platelets</topic><topic>CD16 antigen</topic><topic>CD19 antigen</topic><topic>CD3 antigen</topic><topic>CD3+T lymphocytes</topic><topic>CD4 antigen</topic><topic>CD56 antigen</topic><topic>CD8 antigen</topic><topic>CD8-Positive T-Lymphocytes - immunology</topic><topic>Complement component C3</topic><topic>Complement component C4</topic><topic>cyclosporin</topic><topic>Cyclosporine - therapeutic use</topic><topic>Cyclosporins</topic><topic>Cytokines</topic><topic>Drug dosages</topic><topic>Drug therapy</topic><topic>Female</topic><topic>Females</topic><topic>Flow cytometry</topic><topic>Follow-Up Studies</topic><topic>Globulins</topic><topic>Glucocorticoids</topic><topic>Hematology</topic><topic>Hemorrhage</topic><topic>Hospitals</topic><topic>Humans</topic><topic>Idiopathic thrombocytopenic purpura</topic><topic>immune cell subsets</topic><topic>immune thrombocytopenia</topic><topic>Immunoglobulin A</topic><topic>Immunoglobulin G</topic><topic>Immunology</topic><topic>Immunosuppressive Agents - therapeutic use</topic><topic>Infections</topic><topic>Intravenous administration</topic><topic>Killer Cells, Natural - immunology</topic><topic>Lymphocytes</topic><topic>Lymphocytes B</topic><topic>Lymphocytes T</topic><topic>Male</topic><topic>Medical laboratories</topic><topic>Middle Aged</topic><topic>Patients</topic><topic>Prognosis</topic><topic>Purpura, Thrombocytopenic, Idiopathic - drug therapy</topic><topic>Purpura, Thrombocytopenic, Idiopathic - immunology</topic><topic>Purpura, Thrombocytopenic, Idiopathic - pathology</topic><topic>Retrospective Studies</topic><topic>Thrombocytopenia</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Wang, Ting</creatorcontrib><creatorcontrib>He, Xin</creatorcontrib><creatorcontrib>Ran, Ningyuan</creatorcontrib><creatorcontrib>Liu, Chunyan</creatorcontrib><creatorcontrib>Xing, Limin</creatorcontrib><creatorcontrib>Wang, Huaquan</creatorcontrib><creatorcontrib>Fu, Rong</creatorcontrib><creatorcontrib>Shao, Zonghong</creatorcontrib><collection>Wiley-Blackwell Open Access Collection</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Calcium & Calcified Tissue Abstracts</collection><collection>Immunology Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Public Health Database</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni)</collection><collection>ProQuest Central</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>Natural Science Collection</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Biological Sciences</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Biological Science Database</collection><collection>Publicly Available Content Database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Journal of clinical laboratory analysis</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Wang, Ting</au><au>He, Xin</au><au>Ran, Ningyuan</au><au>Liu, Chunyan</au><au>Xing, Limin</au><au>Wang, Huaquan</au><au>Fu, Rong</au><au>Shao, Zonghong</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Immunological characteristics and effect of cyclosporin in patients with immune thrombocytopenia</atitle><jtitle>Journal of clinical laboratory analysis</jtitle><addtitle>J Clin Lab Anal</addtitle><date>2021-09</date><risdate>2021</risdate><volume>35</volume><issue>9</issue><spage>e23922</spage><epage>n/a</epage><pages>e23922-n/a</pages><issn>0887-8013</issn><eissn>1098-2825</eissn><abstract>Objective
Immune thrombocytopenia (ITP) is well‐known as an antibody‐mediated autoimmune disease, and it is easy to get response but often turns to relapse or refractory. Cyclosporin is a traditional immunosuppressant and had a good effect on ITP patients. In this paper, we retrospectively analyze the immunological characteristics and therapeutic effect of cyclosporin in 220 patients with ITP.
Methods
All newly diagnosed ITP patients in the Department of Hematology, Tianjin Medical University General Hospital from June 2018 to December 2020 were enrolled and divided into four groups according to the expression of autoantibodies and the occurrence of prodromal infection. The basic data and immune indexes of ITP patients in each group were collected. The clinical immunological characteristics of patients in each group and the therapeutic effect of cyclosporin in each group were analyzed.
Results
Multi‐autoantibody ITP patients were more likely to have low serum albumin and high gamma globulin, and the ratio of albumin to globulin decreased. In addition, the level of IgA and IgG increased and the level of complement C3 and C4 decreased more frequently than those in other groups. The number of CD3+T lymphocytes, especially CD3+CD4+T lymphocytes, decreased in ANA+ITP patients. The number of CD16+CD56+NK cells, pDC/DC ratio, and pDC/mDC ratio were higher than those in other groups. The expression of IL‐6 and the proportion of CD19+B lymphocytes increased in two groups of ITP patients with abnormal autoantibodies. The patients of pro‐infected group were more likely to suffer from coagulation disorder. After treatment with cyclosporin, the response rate increased and the 3‐month relapse rate decreased in all ITP patients, and the therapeutic effect of patients with high megakaryocyte number was significantly higher than that of patients with low megakaryocyte number. The impact factors that influence the effect of glucocorticoid and(or) IVIG were the number of CD3+CD8+T lymphocytes, CD4/CD8 cell ratio, and the number of CD19+B lymphocytes. The independent impact factor of cyclosporin therapeutic response rate was the number of CD3+T lymphocytes.
Conclusions
ITP is a heterogeneous disease, recurrence may occur during or rapidly after treatment.
Cyclosporine included treatment can improve the effective rate of ITP and
reduce the relapse rate within 3 months. The number of CD3+T lymphocytes was
the only impact factor that influence the therapeutic effect of
cyclosporin in ITP patients.
We showed clinical characteristics of four subgroups of ITP patients according to immune indexes and proinfection. The patients with autoantibodies usually combined with imbalance of immune cells. Comparing with glucocorticoid and(or) IVIG only treatment, cyclosporin‐included regimen has a higher response rate and lower relapse rate. The number of CD3+T lymphocytes is the independent impact factor that influence the therapeutic effect of cyclosporin.</abstract><cop>United States</cop><pub>John Wiley & Sons, Inc</pub><pmid>34329516</pmid><doi>10.1002/jcla.23922</doi><tpages>10</tpages><orcidid>https://orcid.org/0000-0002-9928-9224</orcidid><oa>free_for_read</oa></addata></record> |
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recordid | cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_8418498 |
source | Wiley-Blackwell Open Access Collection; Open Access: PubMed Central; Publicly Available Content Database |
subjects | Adult Aged Aged, 80 and over Albumin Antibodies antinuclear antibodies Autoantibodies Autoimmune diseases B-Lymphocytes - immunology Blood platelets CD16 antigen CD19 antigen CD3 antigen CD3+T lymphocytes CD4 antigen CD56 antigen CD8 antigen CD8-Positive T-Lymphocytes - immunology Complement component C3 Complement component C4 cyclosporin Cyclosporine - therapeutic use Cyclosporins Cytokines Drug dosages Drug therapy Female Females Flow cytometry Follow-Up Studies Globulins Glucocorticoids Hematology Hemorrhage Hospitals Humans Idiopathic thrombocytopenic purpura immune cell subsets immune thrombocytopenia Immunoglobulin A Immunoglobulin G Immunology Immunosuppressive Agents - therapeutic use Infections Intravenous administration Killer Cells, Natural - immunology Lymphocytes Lymphocytes B Lymphocytes T Male Medical laboratories Middle Aged Patients Prognosis Purpura, Thrombocytopenic, Idiopathic - drug therapy Purpura, Thrombocytopenic, Idiopathic - immunology Purpura, Thrombocytopenic, Idiopathic - pathology Retrospective Studies Thrombocytopenia |
title | Immunological characteristics and effect of cyclosporin in patients with immune thrombocytopenia |
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