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CAR/CXCR5-T cell immunotherapy is safe and potentially efficacious in promoting sustained remission of SIV infection

PLoS Pathogens(2022)10.1371/journal.ppat.1009831Source: DataRank Database

CAR/CXCR5-T cell immunotherapy is safe and potentially efficacious in promoting sustained remission of SIV infection is a research paper published in PLoS Pathogens (2022). On theSindex it has a DataRank of 0. It has been cited 42 times.

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Open Access42 citations

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›Methodology & internals

datarank_citation_only_1hop_v6· scope data_onlyMethodology

Pipeline:MetadataData-paper checkEnrichmentCitation networkScoring

Enrichment:Funding (22 grants)OA: goldTopics (52)IDs (PubMed)SDGs (1)

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Reusable (0/3)

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Authors (12)

Hadia M. Abdelaal ORCID,Emily K. Cartwright ORCID,Jhomary Molden ORCID,Brianna C. Davey ORCID,Jordan D. Sauve

Live enrichment

PubMed:35130312

national institutes of health

Grant: 5R01AI096966-06S1

national institutes of health

Grant: 1UM1AI26617

national institutes of health

Grant: P51OD011106/P51RR000167

national institutes of health

Grant: 5U01HL127479-03

MIN-REACH Research Evaluation and Commercialization Hub

national institutes of health

Grant: R01AI143380

national institutes of health

Grant: 1UM14126617

national institutes of health

Grant: 5-T32 AI 55433

National Institutes of Health

Grant: Intramural AIDS Targeted Antiviral Program

National Institutes of Health

Grant: 5T32AI055433-08

Infectious Disease Training in Clinical Investigation

National Institutes of Health

Grant: 3P51OD011106-60S1

Wisconsin National Primate Research Center Support

National Institutes of Health

Grant: 7R24OD010976-14

Resource for Nonhuman Primate Cell Depleting Antibodies

National Institutes of Health

Grant: 5R01AI096966-06

Mechanisms Underlying Persistent Lentivirus Replication in Follicular T Cells

National Institutes of Health

Grant: 3U24AI126683-09S1

Nonhuman Primate Reagent Resource

National Institutes of Health

Grant: 5R01AI143380-04

Targeting virus-specific CAR T cells to lymphoid follicles to achieve durable HIV suppression

NCRR NIH HHS

Grant: P51 RR000167

NIAID NIH HHS

Grant: U24 AI126683

NIAID NIH HHS

Grant: R01 AI096966

NIDA NIH HHS

Grant: T32 DA007097

NHLBI NIH HHS

Grant: U01 HL127479

NIH HHS

Grant: R24 OD010976

NIAID NIH HHS

Grant: T32 AI055433

NIH HHS

Grant: P51 OD011106

goldLicense: cc-by

publisherhttps://doi.org/10.1371/journal.ppat.1009831

publisherhttps://dx.plos.org/10.1371/journal.ppat.1009831

repositoryhttp://hdl.handle.net/10150/663677

repositoryhttps://doaj.org/article/ec02b79848574b81a11bd4e2ead3af63

repositoryhttps://www.ncbi.nlm.nih.gov/pmc/articles/8853520

Fields of Study

0301 basic medicine03 medical and health sciencesAnimalsB-LymphocytesCD4-Positive T-LymphocytesCD8-Positive T-LymphocytesGerminal CenterHumansImmunotherapyLymph NodesMacaca mulattaRNA, ViralReceptors, CXCR5Receptors, Chimeric AntigenSimian Acquired Immunodeficiency SyndromeSimian Immunodeficiency VirusViral Load

MeSH Terms

AnimalsB-LymphocytesCD4-Positive T-LymphocytesCD8-Positive T-LymphocytesGerminal CenterHumansImmunotherapyLymph NodesMacaca mulattaRNA, ViralReceptors, CXCR5Receptors, Chimeric AntigenSimian Acquired Immunodeficiency SyndromeSimian Immunodeficiency VirusViral Load

Keywords

CD4-Positive T-LymphocytesReceptors, CXCR5B-LymphocytesReceptors, Chimeric AntigenQH301-705.5Simian Acquired Immunodeficiency SyndromeRC581-607CD8-Positive T-LymphocytesViral LoadGerminal CenterMacaca mulattaAnimalsHumansRNA, ViralSimian Immunodeficiency VirusImmunotherapyLymph NodesImmunologic diseases. AllergyBiology (General)Research Article

Sustainable Development Goals

SDG 3: 3. Good health