Loading…
Functional investigation of chimeric antigen receptor T cells targeting LMP1 antigen
This study aimed to create a type of CAR-T cells that targets LMP1 antigen and study its immunotherapeutic effect on LMP1-positive hematological malignancies. To generate LMP1 CAR-T cells, a plasmid expressing LMP1 CAR was created using molecular cloning technology, and T cells were infected with LM...
Saved in:
Published in: | Zhōnghuá xuèyèxué zázhì 2022-03, Vol.43 (3), p.229-234 |
---|---|
Main Authors: | , , , , , , , , , |
Format: | Article |
Language: | Chinese |
Subjects: | |
Online Access: | Get full text |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
cited_by | |
---|---|
cites | |
container_end_page | 234 |
container_issue | 3 |
container_start_page | 229 |
container_title | Zhōnghuá xuèyèxué zázhì |
container_volume | 43 |
creator | He, H Z Xing, Y Y Zhang, Y Xu, Y X Tian, Z Xing, H Y Tang, K J Rao, Q Wang, J X Wang, M |
description | This study aimed to create a type of CAR-T cells that targets LMP1 antigen and study its immunotherapeutic effect on LMP1-positive hematological malignancies.
To generate LMP1 CAR-T cells, a plasmid expressing LMP1 CAR was created using molecular cloning technology, and T cells were infected with LMP1 CAR lentivirus. The effects of LMP1 CAR-T cells on specific cytotoxicity against LMP1-positive tumor cell lines infected with the EB virus had been confirmed.
① LMP1 protein expressing on EB virus-positive lymphoma cells surface was verified. ② The LMP1 CAR-expressing plasmid was created, and LMP1 CAR-T cells were obtained by infecting T cells with a lentivirus packaging system, with an infection efficiency of more than 80% . ③LMP1 CAR-T cells have a 4∶1 effect-to-target ratio in killing LMP1-positive lymphoma cells. The killing effect of LMP1 CAR-T cells on Raji cells was enhanced after 48 h of coculture, but there was no significant killing effect on Ramos, which are LMP1-negative lymphoma cells. ④After cocult |
doi_str_mv | 10.3760/cma.j.issn.0253-2727.2022.03.008 |
format | article |
fullrecord | <record><control><sourceid>proquest_pubme</sourceid><recordid>TN_cdi_proquest_miscellaneous_2649592968</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>2649592968</sourcerecordid><originalsourceid>FETCH-LOGICAL-p126t-5fc481c72bd45091cb64f6ca70186ccce1c50aaa6bf1c06aa6e6903bd0a4ed953</originalsourceid><addsrcrecordid>eNo9kMFOwzAQRH0A0ar0F5CPvcSs7dhJjqiigFQEh3KOnI1TjBIn2AkSf08qKKedHT2tZoeQDQcmMw232Bn2wVyMnoFQMhGZyJgAIRhIBpBfkOW_vyDrGF0FikudSwlXZCFVCirL-ZIcdpPH0fXetNT5LxtHdzSnnfYNxXfX2eCQGj_b1tNg0Q5jH-iBom3bSEcTjnZ0_kj3z6_8zF2Ty8a00a7_5oq87e4P28dk__LwtL3bJwMXekxUg2nOMRNVnSooOFY6bTSaDHiuEdFyVGCM0VXDEfQsrC5AVjWY1NaFkiuy-b07hP5zmrOXnYunYMbbfoql0GmhClHMb6_IzR86VZ2tyyG4zoTv8tyE_AHir2S3</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2649592968</pqid></control><display><type>article</type><title>Functional investigation of chimeric antigen receptor T cells targeting LMP1 antigen</title><source>PubMed Central</source><creator>He, H Z ; Xing, Y Y ; Zhang, Y ; Xu, Y X ; Tian, Z ; Xing, H Y ; Tang, K J ; Rao, Q ; Wang, J X ; Wang, M</creator><creatorcontrib>He, H Z ; Xing, Y Y ; Zhang, Y ; Xu, Y X ; Tian, Z ; Xing, H Y ; Tang, K J ; Rao, Q ; Wang, J X ; Wang, M</creatorcontrib><description>This study aimed to create a type of CAR-T cells that targets LMP1 antigen and study its immunotherapeutic effect on LMP1-positive hematological malignancies.
To generate LMP1 CAR-T cells, a plasmid expressing LMP1 CAR was created using molecular cloning technology, and T cells were infected with LMP1 CAR lentivirus. The effects of LMP1 CAR-T cells on specific cytotoxicity against LMP1-positive tumor cell lines infected with the EB virus had been confirmed.
① LMP1 protein expressing on EB virus-positive lymphoma cells surface was verified. ② The LMP1 CAR-expressing plasmid was created, and LMP1 CAR-T cells were obtained by infecting T cells with a lentivirus packaging system, with an infection efficiency of more than 80% . ③LMP1 CAR-T cells have a 4∶1 effect-to-target ratio in killing LMP1-positive lymphoma cells. The killing effect of LMP1 CAR-T cells on Raji cells was enhanced after 48 h of coculture, but there was no significant killing effect on Ramos, which are LMP1-negative lymphoma cells. ④After cocult</description><identifier>ISSN: 0253-2727</identifier><identifier>DOI: 10.3760/cma.j.issn.0253-2727.2022.03.008</identifier><identifier>PMID: 35405781</identifier><language>chi</language><publisher>China</publisher><subject>Cell Line, Tumor ; Herpesvirus 4, Human ; Humans ; Lentivirus ; Lymphoma - therapy ; Receptors, Chimeric Antigen - genetics ; T-Lymphocytes ; Viral Matrix Proteins</subject><ispartof>Zhōnghuá xuèyèxué zázhì, 2022-03, Vol.43 (3), p.229-234</ispartof><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/35405781$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>He, H Z</creatorcontrib><creatorcontrib>Xing, Y Y</creatorcontrib><creatorcontrib>Zhang, Y</creatorcontrib><creatorcontrib>Xu, Y X</creatorcontrib><creatorcontrib>Tian, Z</creatorcontrib><creatorcontrib>Xing, H Y</creatorcontrib><creatorcontrib>Tang, K J</creatorcontrib><creatorcontrib>Rao, Q</creatorcontrib><creatorcontrib>Wang, J X</creatorcontrib><creatorcontrib>Wang, M</creatorcontrib><title>Functional investigation of chimeric antigen receptor T cells targeting LMP1 antigen</title><title>Zhōnghuá xuèyèxué zázhì</title><addtitle>Zhonghua Xue Ye Xue Za Zhi</addtitle><description>This study aimed to create a type of CAR-T cells that targets LMP1 antigen and study its immunotherapeutic effect on LMP1-positive hematological malignancies.
To generate LMP1 CAR-T cells, a plasmid expressing LMP1 CAR was created using molecular cloning technology, and T cells were infected with LMP1 CAR lentivirus. The effects of LMP1 CAR-T cells on specific cytotoxicity against LMP1-positive tumor cell lines infected with the EB virus had been confirmed.
① LMP1 protein expressing on EB virus-positive lymphoma cells surface was verified. ② The LMP1 CAR-expressing plasmid was created, and LMP1 CAR-T cells were obtained by infecting T cells with a lentivirus packaging system, with an infection efficiency of more than 80% . ③LMP1 CAR-T cells have a 4∶1 effect-to-target ratio in killing LMP1-positive lymphoma cells. The killing effect of LMP1 CAR-T cells on Raji cells was enhanced after 48 h of coculture, but there was no significant killing effect on Ramos, which are LMP1-negative lymphoma cells. ④After cocult</description><subject>Cell Line, Tumor</subject><subject>Herpesvirus 4, Human</subject><subject>Humans</subject><subject>Lentivirus</subject><subject>Lymphoma - therapy</subject><subject>Receptors, Chimeric Antigen - genetics</subject><subject>T-Lymphocytes</subject><subject>Viral Matrix Proteins</subject><issn>0253-2727</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2022</creationdate><recordtype>article</recordtype><recordid>eNo9kMFOwzAQRH0A0ar0F5CPvcSs7dhJjqiigFQEh3KOnI1TjBIn2AkSf08qKKedHT2tZoeQDQcmMw232Bn2wVyMnoFQMhGZyJgAIRhIBpBfkOW_vyDrGF0FikudSwlXZCFVCirL-ZIcdpPH0fXetNT5LxtHdzSnnfYNxXfX2eCQGj_b1tNg0Q5jH-iBom3bSEcTjnZ0_kj3z6_8zF2Ty8a00a7_5oq87e4P28dk__LwtL3bJwMXekxUg2nOMRNVnSooOFY6bTSaDHiuEdFyVGCM0VXDEfQsrC5AVjWY1NaFkiuy-b07hP5zmrOXnYunYMbbfoql0GmhClHMb6_IzR86VZ2tyyG4zoTv8tyE_AHir2S3</recordid><startdate>20220314</startdate><enddate>20220314</enddate><creator>He, H Z</creator><creator>Xing, Y Y</creator><creator>Zhang, Y</creator><creator>Xu, Y X</creator><creator>Tian, Z</creator><creator>Xing, H Y</creator><creator>Tang, K J</creator><creator>Rao, Q</creator><creator>Wang, J X</creator><creator>Wang, M</creator><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>7X8</scope></search><sort><creationdate>20220314</creationdate><title>Functional investigation of chimeric antigen receptor T cells targeting LMP1 antigen</title><author>He, H Z ; Xing, Y Y ; Zhang, Y ; Xu, Y X ; Tian, Z ; Xing, H Y ; Tang, K J ; Rao, Q ; Wang, J X ; Wang, M</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-p126t-5fc481c72bd45091cb64f6ca70186ccce1c50aaa6bf1c06aa6e6903bd0a4ed953</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>chi</language><creationdate>2022</creationdate><topic>Cell Line, Tumor</topic><topic>Herpesvirus 4, Human</topic><topic>Humans</topic><topic>Lentivirus</topic><topic>Lymphoma - therapy</topic><topic>Receptors, Chimeric Antigen - genetics</topic><topic>T-Lymphocytes</topic><topic>Viral Matrix Proteins</topic><toplevel>online_resources</toplevel><creatorcontrib>He, H Z</creatorcontrib><creatorcontrib>Xing, Y Y</creatorcontrib><creatorcontrib>Zhang, Y</creatorcontrib><creatorcontrib>Xu, Y X</creatorcontrib><creatorcontrib>Tian, Z</creatorcontrib><creatorcontrib>Xing, H Y</creatorcontrib><creatorcontrib>Tang, K J</creatorcontrib><creatorcontrib>Rao, Q</creatorcontrib><creatorcontrib>Wang, J X</creatorcontrib><creatorcontrib>Wang, M</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>MEDLINE - Academic</collection><jtitle>Zhōnghuá xuèyèxué zázhì</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>He, H Z</au><au>Xing, Y Y</au><au>Zhang, Y</au><au>Xu, Y X</au><au>Tian, Z</au><au>Xing, H Y</au><au>Tang, K J</au><au>Rao, Q</au><au>Wang, J X</au><au>Wang, M</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Functional investigation of chimeric antigen receptor T cells targeting LMP1 antigen</atitle><jtitle>Zhōnghuá xuèyèxué zázhì</jtitle><addtitle>Zhonghua Xue Ye Xue Za Zhi</addtitle><date>2022-03-14</date><risdate>2022</risdate><volume>43</volume><issue>3</issue><spage>229</spage><epage>234</epage><pages>229-234</pages><issn>0253-2727</issn><abstract>This study aimed to create a type of CAR-T cells that targets LMP1 antigen and study its immunotherapeutic effect on LMP1-positive hematological malignancies.
To generate LMP1 CAR-T cells, a plasmid expressing LMP1 CAR was created using molecular cloning technology, and T cells were infected with LMP1 CAR lentivirus. The effects of LMP1 CAR-T cells on specific cytotoxicity against LMP1-positive tumor cell lines infected with the EB virus had been confirmed.
① LMP1 protein expressing on EB virus-positive lymphoma cells surface was verified. ② The LMP1 CAR-expressing plasmid was created, and LMP1 CAR-T cells were obtained by infecting T cells with a lentivirus packaging system, with an infection efficiency of more than 80% . ③LMP1 CAR-T cells have a 4∶1 effect-to-target ratio in killing LMP1-positive lymphoma cells. The killing effect of LMP1 CAR-T cells on Raji cells was enhanced after 48 h of coculture, but there was no significant killing effect on Ramos, which are LMP1-negative lymphoma cells. ④After cocult</abstract><cop>China</cop><pmid>35405781</pmid><doi>10.3760/cma.j.issn.0253-2727.2022.03.008</doi><tpages>6</tpages></addata></record> |
fulltext | fulltext |
identifier | ISSN: 0253-2727 |
ispartof | Zhōnghuá xuèyèxué zázhì, 2022-03, Vol.43 (3), p.229-234 |
issn | 0253-2727 |
language | chi |
recordid | cdi_proquest_miscellaneous_2649592968 |
source | PubMed Central |
subjects | Cell Line, Tumor Herpesvirus 4, Human Humans Lentivirus Lymphoma - therapy Receptors, Chimeric Antigen - genetics T-Lymphocytes Viral Matrix Proteins |
title | Functional investigation of chimeric antigen receptor T cells targeting LMP1 antigen |
url | http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-08T02%3A44%3A38IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_pubme&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Functional%20investigation%20of%20chimeric%20antigen%20receptor%20T%20cells%20targeting%20LMP1%20antigen&rft.jtitle=Zh%C5%8Dnghu%C3%A1%20xu%C3%A8y%C3%A8xu%C3%A9%20z%C3%A1zh%C3%AC&rft.au=He,%20H%20Z&rft.date=2022-03-14&rft.volume=43&rft.issue=3&rft.spage=229&rft.epage=234&rft.pages=229-234&rft.issn=0253-2727&rft_id=info:doi/10.3760/cma.j.issn.0253-2727.2022.03.008&rft_dat=%3Cproquest_pubme%3E2649592968%3C/proquest_pubme%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-p126t-5fc481c72bd45091cb64f6ca70186ccce1c50aaa6bf1c06aa6e6903bd0a4ed953%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=2649592968&rft_id=info:pmid/35405781&rfr_iscdi=true |