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High percentage of bone marrow CD8 + tissue-resident-like memory T cells predicts inferior survival in patients with acute myeloid leukemia
Tissue-resident memory T (TRM) cells infiltrating solid tumors could influence tumor progression and the response to immune therapies. However, the proportion and prognostic value of TRM cells in the bone marrow (BM) of patients with acute myeloid leukemia (AML) are unclear. In this study, we used f...
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Published in: | Blood science 2024-07, Vol.6 (3), p.e00194-e00194 |
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creator | Cai, Letong Lai, Wenpu Yao, Danlin Gu, Yinfeng Liang, Chaofeng Liu, Lian Lai, Jing Yu, Zhi Zha, Xianfeng Yu, Xibao Wu, Xiuli Chen, Shaohua Luo, Oscar Junhong Li, Yangqiu Wang, Chunyan Qin, Pengfei Huang, Xin Xu, Ling |
description | Tissue-resident memory T (TRM) cells infiltrating solid tumors could influence tumor progression and the response to immune therapies. However, the proportion and prognostic value of TRM cells in the bone marrow (BM) of patients with acute myeloid leukemia (AML) are unclear. In this study, we used flow cytometry to assay the phenotype of 49 BM samples from patients newly diagnosed with AML (ND-AML). We found that the BM CD8
effector memory (TEM) cells highly expressed CD69 (CD8
TRM-like T cells), and their percentage was significantly increased in patients with ND-AML compared with that in healthy individuals (HI). The high percentage of CD8
TRM-like subset was associated with poor overall survival in our ND-AML cohort. The Kaplan-Meier Plotter database verified a significantly reduced survival rate among patients with high expression of CD8
TRM-like T cell characteristic genes (
,
, and
), especially the M4 and M5 subtypes. Phenotypic analysis revealed that the BM CD8
TRM-like subpopulation exhibited exhausted T cell characteristics, but its high expression of CD27 and CD28 and low expression of CD57 suggested its high proliferative potential. The single-cell proteogenomic dataset confirmed the existence of TRM-like CD8
T cells in the BM of patients with AML and verified the high expression of immune checkpoints and costimulatory molecules. In conclusion, we found that the accumulation of BM CD8
TRM-like cells could be an immune-related survival prediction marker for patients with AML. |
doi_str_mv | 10.1097/BS9.0000000000000194 |
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effector memory (TEM) cells highly expressed CD69 (CD8
TRM-like T cells), and their percentage was significantly increased in patients with ND-AML compared with that in healthy individuals (HI). The high percentage of CD8
TRM-like subset was associated with poor overall survival in our ND-AML cohort. The Kaplan-Meier Plotter database verified a significantly reduced survival rate among patients with high expression of CD8
TRM-like T cell characteristic genes (
,
, and
), especially the M4 and M5 subtypes. Phenotypic analysis revealed that the BM CD8
TRM-like subpopulation exhibited exhausted T cell characteristics, but its high expression of CD27 and CD28 and low expression of CD57 suggested its high proliferative potential. The single-cell proteogenomic dataset confirmed the existence of TRM-like CD8
T cells in the BM of patients with AML and verified the high expression of immune checkpoints and costimulatory molecules. In conclusion, we found that the accumulation of BM CD8
TRM-like cells could be an immune-related survival prediction marker for patients with AML.</description><identifier>ISSN: 2543-6368</identifier><identifier>EISSN: 2543-6368</identifier><identifier>DOI: 10.1097/BS9.0000000000000194</identifier><identifier>PMID: 38854481</identifier><language>eng</language><publisher>United States: Lippincott Williams & Wilkins</publisher><ispartof>Blood science, 2024-07, Vol.6 (3), p.e00194-e00194</ispartof><rights>Copyright © 2024 The Authors. Published by Wolters Kluwer Health Inc., on behalf of the Chinese Medical Association (CMA) and Institute of Hematology, Chinese Academy of Medical Sciences & Peking Union Medical College (IHCAMS).</rights><rights>Copyright © 2024 The Authors. Published by Wolters Kluwer Health Inc., on behalf of the Chinese Medical Association (CMA) and Institute of Hematology, Chinese Academy of Medical Sciences & Peking Union Medical College (IHCAMS). 2024</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c354t-5828ae71c0c63aa89427f4f82c47b2f9a7e69d702dcd00df1392ea6d79242d273</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC11161300/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC11161300/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,27924,27925,53791,53793</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/38854481$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Cai, Letong</creatorcontrib><creatorcontrib>Lai, Wenpu</creatorcontrib><creatorcontrib>Yao, Danlin</creatorcontrib><creatorcontrib>Gu, Yinfeng</creatorcontrib><creatorcontrib>Liang, Chaofeng</creatorcontrib><creatorcontrib>Liu, Lian</creatorcontrib><creatorcontrib>Lai, Jing</creatorcontrib><creatorcontrib>Yu, Zhi</creatorcontrib><creatorcontrib>Zha, Xianfeng</creatorcontrib><creatorcontrib>Yu, Xibao</creatorcontrib><creatorcontrib>Wu, Xiuli</creatorcontrib><creatorcontrib>Chen, Shaohua</creatorcontrib><creatorcontrib>Luo, Oscar Junhong</creatorcontrib><creatorcontrib>Li, Yangqiu</creatorcontrib><creatorcontrib>Wang, Chunyan</creatorcontrib><creatorcontrib>Qin, Pengfei</creatorcontrib><creatorcontrib>Huang, Xin</creatorcontrib><creatorcontrib>Xu, Ling</creatorcontrib><title>High percentage of bone marrow CD8 + tissue-resident-like memory T cells predicts inferior survival in patients with acute myeloid leukemia</title><title>Blood science</title><addtitle>Blood Sci</addtitle><description>Tissue-resident memory T (TRM) cells infiltrating solid tumors could influence tumor progression and the response to immune therapies. However, the proportion and prognostic value of TRM cells in the bone marrow (BM) of patients with acute myeloid leukemia (AML) are unclear. In this study, we used flow cytometry to assay the phenotype of 49 BM samples from patients newly diagnosed with AML (ND-AML). We found that the BM CD8
effector memory (TEM) cells highly expressed CD69 (CD8
TRM-like T cells), and their percentage was significantly increased in patients with ND-AML compared with that in healthy individuals (HI). The high percentage of CD8
TRM-like subset was associated with poor overall survival in our ND-AML cohort. The Kaplan-Meier Plotter database verified a significantly reduced survival rate among patients with high expression of CD8
TRM-like T cell characteristic genes (
,
, and
), especially the M4 and M5 subtypes. Phenotypic analysis revealed that the BM CD8
TRM-like subpopulation exhibited exhausted T cell characteristics, but its high expression of CD27 and CD28 and low expression of CD57 suggested its high proliferative potential. The single-cell proteogenomic dataset confirmed the existence of TRM-like CD8
T cells in the BM of patients with AML and verified the high expression of immune checkpoints and costimulatory molecules. In conclusion, we found that the accumulation of BM CD8
TRM-like cells could be an immune-related survival prediction marker for patients with AML.</description><issn>2543-6368</issn><issn>2543-6368</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2024</creationdate><recordtype>article</recordtype><sourceid>DOA</sourceid><recordid>eNpdks1u1DAUhSMEolXpGyDkJRJK8V_8s0IwFFqpEou2a8tj38y4TeJgJ1PNM_DS9TClmuKNretzvmtfnap6T_AZwVp-_natz_DhIpq_qo5pw1ktmFCvD85H1WnOd0VDGWGS8bfVEVOq4VyR4-rPRVit0QjJwTDZFaDYomUcAPU2pfiAFt8V-oSmkPMMdYIcfNHVXbgvCuhj2qIb5KDrMhoT-OCmjMLQQgoxoTynTdjYrlTQaKdQnBk9hGmNrJunAthCF4NHHcz30Af7rnrT2i7D6dN-Ut3-OL9ZXNRXv35eLr5e1Y41fKobRZUFSRx2glmrNKey5a2ijsslbbWVILSXmHrnMfYtYZqCFV5qyqmnkp1Ul3uuj_bOjCmUv25NtMH8LcS0MjZNwXVgPCsEKbSmlHDmrJa0YQ1TIBvSeI0L68ueNc7LHvxuisl2L6Avb4awNqu4MYQQQQq9ED4-EVL8PUOeTB_ybqR2gDhnw7AQjAlMdZHyvdSlmHOC9rkPwWaXC1NyYf7PRbF9OHzjs-lfCtgj7120Ig</recordid><startdate>20240701</startdate><enddate>20240701</enddate><creator>Cai, Letong</creator><creator>Lai, Wenpu</creator><creator>Yao, Danlin</creator><creator>Gu, Yinfeng</creator><creator>Liang, Chaofeng</creator><creator>Liu, Lian</creator><creator>Lai, Jing</creator><creator>Yu, Zhi</creator><creator>Zha, Xianfeng</creator><creator>Yu, Xibao</creator><creator>Wu, Xiuli</creator><creator>Chen, Shaohua</creator><creator>Luo, Oscar Junhong</creator><creator>Li, Yangqiu</creator><creator>Wang, Chunyan</creator><creator>Qin, Pengfei</creator><creator>Huang, Xin</creator><creator>Xu, Ling</creator><general>Lippincott Williams & Wilkins</general><general>Wolters Kluwer Health</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>5PM</scope><scope>DOA</scope></search><sort><creationdate>20240701</creationdate><title>High percentage of bone marrow CD8 + tissue-resident-like memory T cells predicts inferior survival in patients with acute myeloid leukemia</title><author>Cai, Letong ; Lai, Wenpu ; Yao, Danlin ; Gu, Yinfeng ; Liang, Chaofeng ; Liu, Lian ; Lai, Jing ; Yu, Zhi ; Zha, Xianfeng ; Yu, Xibao ; Wu, Xiuli ; Chen, Shaohua ; Luo, Oscar Junhong ; Li, Yangqiu ; Wang, Chunyan ; Qin, Pengfei ; Huang, Xin ; Xu, Ling</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c354t-5828ae71c0c63aa89427f4f82c47b2f9a7e69d702dcd00df1392ea6d79242d273</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2024</creationdate><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Cai, Letong</creatorcontrib><creatorcontrib>Lai, Wenpu</creatorcontrib><creatorcontrib>Yao, Danlin</creatorcontrib><creatorcontrib>Gu, Yinfeng</creatorcontrib><creatorcontrib>Liang, Chaofeng</creatorcontrib><creatorcontrib>Liu, Lian</creatorcontrib><creatorcontrib>Lai, Jing</creatorcontrib><creatorcontrib>Yu, Zhi</creatorcontrib><creatorcontrib>Zha, Xianfeng</creatorcontrib><creatorcontrib>Yu, Xibao</creatorcontrib><creatorcontrib>Wu, Xiuli</creatorcontrib><creatorcontrib>Chen, Shaohua</creatorcontrib><creatorcontrib>Luo, Oscar Junhong</creatorcontrib><creatorcontrib>Li, Yangqiu</creatorcontrib><creatorcontrib>Wang, Chunyan</creatorcontrib><creatorcontrib>Qin, Pengfei</creatorcontrib><creatorcontrib>Huang, Xin</creatorcontrib><creatorcontrib>Xu, Ling</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><collection>DOAJ Directory of Open Access Journals</collection><jtitle>Blood science</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Cai, Letong</au><au>Lai, Wenpu</au><au>Yao, Danlin</au><au>Gu, Yinfeng</au><au>Liang, Chaofeng</au><au>Liu, Lian</au><au>Lai, Jing</au><au>Yu, Zhi</au><au>Zha, Xianfeng</au><au>Yu, Xibao</au><au>Wu, Xiuli</au><au>Chen, Shaohua</au><au>Luo, Oscar Junhong</au><au>Li, Yangqiu</au><au>Wang, Chunyan</au><au>Qin, Pengfei</au><au>Huang, Xin</au><au>Xu, Ling</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>High percentage of bone marrow CD8 + tissue-resident-like memory T cells predicts inferior survival in patients with acute myeloid leukemia</atitle><jtitle>Blood science</jtitle><addtitle>Blood Sci</addtitle><date>2024-07-01</date><risdate>2024</risdate><volume>6</volume><issue>3</issue><spage>e00194</spage><epage>e00194</epage><pages>e00194-e00194</pages><issn>2543-6368</issn><eissn>2543-6368</eissn><abstract>Tissue-resident memory T (TRM) cells infiltrating solid tumors could influence tumor progression and the response to immune therapies. However, the proportion and prognostic value of TRM cells in the bone marrow (BM) of patients with acute myeloid leukemia (AML) are unclear. In this study, we used flow cytometry to assay the phenotype of 49 BM samples from patients newly diagnosed with AML (ND-AML). We found that the BM CD8
effector memory (TEM) cells highly expressed CD69 (CD8
TRM-like T cells), and their percentage was significantly increased in patients with ND-AML compared with that in healthy individuals (HI). The high percentage of CD8
TRM-like subset was associated with poor overall survival in our ND-AML cohort. The Kaplan-Meier Plotter database verified a significantly reduced survival rate among patients with high expression of CD8
TRM-like T cell characteristic genes (
,
, and
), especially the M4 and M5 subtypes. Phenotypic analysis revealed that the BM CD8
TRM-like subpopulation exhibited exhausted T cell characteristics, but its high expression of CD27 and CD28 and low expression of CD57 suggested its high proliferative potential. The single-cell proteogenomic dataset confirmed the existence of TRM-like CD8
T cells in the BM of patients with AML and verified the high expression of immune checkpoints and costimulatory molecules. In conclusion, we found that the accumulation of BM CD8
TRM-like cells could be an immune-related survival prediction marker for patients with AML.</abstract><cop>United States</cop><pub>Lippincott Williams & Wilkins</pub><pmid>38854481</pmid><doi>10.1097/BS9.0000000000000194</doi><oa>free_for_read</oa></addata></record> |
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title | High percentage of bone marrow CD8 + tissue-resident-like memory T cells predicts inferior survival in patients with acute myeloid leukemia |
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