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Redundancy in Innate Immune Pathways That Promote CD8+ T-Cell Responses in AAV1 Muscle Gene Transfer

Viruses(2024)10.3390/v16101507Source: DataRank Database

Redundancy in Innate Immune Pathways That Promote CD8+ T-Cell Responses in AAV1 Muscle Gene Transfer is a research paper published in Viruses (2024). On theSindex it has a DataRank of 0. It has been cited 11 times.

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Open Access11 citations

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›Methodology & internals

datarank_citation_only_1hop_v6· scope data_onlyMethodology

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Enrichment:Funding (18 grants)Impact (FWCI 4.27)OA: goldTopics (52)IDs (PubMed, PMC, OpenAlex)

FAIR Checklist

Context only (not used in score)

Findable (1/2)

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Accessible (1/2)

Open Access

Interoperable (0/2)

Reusable (0/3)

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Authors (10)

Sandeep Kumar ORCID,Di Cao ORCID,Maite Muñoz-Melero,Sreevani Arisa,Bridget A. Brian

Live enrichment

PubMed:39459842 PMC:PMC11512359 OpenAlex:https://openalex.org/W4402776364

Riley Children’s Foundation

Grant: R01 AI51390

Riley Children’s Foundation

Grant: R01 HL131093

Riley Children’s Foundation

Grant: R01 AI177600

Riley Children’s Foundation

Grant: R01 NS131416

Riley Children’s Foundation

Grant: T32 AI060519

Riley Children’s Foundation

Grant: P30 CA082709

Riley Children’s Foundation

Grant: U54 DK106846

Riley Children’s Foundation

Grant: 1S10D012270

NIH/NIAID

Grant: AI51390

NIH HHS

Grant: S10 OD012270

NIAID NIH HHS

Grant: R01 AI051390

National Institutes of Health

Grant: 1R01HL131093-01A1

Enhancing immune regulation in gene therapy for hemophilia

National Institutes of Health

Grant: 5T32AI060519-14

Immunology and Infectious Diseases

National Institutes of Health

Grant: 7R01AI051390-05

Immunology of Factor IX Gene Transfer to Liver

National Institutes of Health

Grant: 5R01AI177600-02

Mechanism of immune response to muscle-directed AAV gene transfer

National Institutes of Health

Grant: 3P30CA082709-16S3

Indiana University Melvin and Bren Simon Cancer Center Support Grant

National Institutes of Health

Grant: 5U54DK106846-03

Hematopoietic stem and progenitor cell regulation for enhanced clinical efficacy

National Institutes of Health

Grant: 1R01NS131416-01

CRISPR editing therapy for Duchenne muscular dystrophy

FWCI

4.27

Citation Percentile

0.9%

Citation Trend

2025

2026

goldLicense: cc-by

journalhttps://www.mdpi.com/1999-4915/16/10/1507/pdf

GOLDhttps://doi.org/10.3390/v16101507

publisherhttps://www.mdpi.com/1999-4915/16/10/1507/pdf

repositoryhttps://pubmed.ncbi.nlm.nih.gov/39459842

repositoryhttps://hdl.handle.net/1805/44521

Fields of Study

Virus-based gene therapy researchCAR-T cell therapy researchViral Infections and Immunology ResearchMedicineBiology0301 basic medicine03 medical and health sciences

MeSH Terms

DependovirusAnimalsGenetic VectorsImmunity, InnateMice, Inbred C57BLSignal TransductionGene Transfer TechniquesCD8-Positive T-LymphocytesMuscle, SkeletalTransgenesToll-Like Receptor 9MiceMyeloid Differentiation Factor 88

Keywords

Innate immune systemImmune systemGene transferImmunologyCD8Cell biologyBiologyT cellGeneGeneticsMuscleIL-1Adeno-associated virusTLR9Cd8 T CellGenetic Vectors610CD8-Positive T-LymphocytesMicrobiologyArticleMiceAnimalsTransgenesMuscle, SkeletalGene Transfer TechniquesDependovirusQR1-502Immunity, InnateMice, Inbred C57BLToll-Like Receptor 9Myeloid Differentiation Factor 88Signal Transduction