نتائج البحث - "Moorman, Cody D."

1

Academic Journal

CAR-T cells and CAR-Tregs targeting conventional type-1 dendritic cell suppress experimental autoimmune encephalomyelitis

المؤلفون: Moorman, Cody D., Yu, Sherman, Briseno, Carlos G., Phee, Hyewon, Sahoo, Anupama, Ramrakhiani, Ambika, Chaudhry, Ashutosh

المصدر: Frontiers in Immunology ; volume 14 ; ISSN 1664-3224

الاتاحة: http://dx.doi.org/10.3389/fimmu.2023.1235222
https://www.frontiersin.org/articles/10.3389/fimmu.2023.1235222/full

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2

Academic Journal

Emerging Therapeutics for Immune Tolerance: Tolerogenic Vaccines, T cell Therapy, and IL-2 Therapy

المؤلفون: Moorman, Cody D., Sohn, Sue J., Phee, Hyewon

المصدر: Frontiers in Immunology ; volume 12 ; ISSN 1664-3224

الاتاحة: http://dx.doi.org/10.3389/fimmu.2021.657768
https://www.frontiersin.org/articles/10.3389/fimmu.2021.657768/full

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3

Academic Journal

A GM-CSF-neuroantigen tolerogenic vaccine elicits inefficient antigen recognition events below the CD40L triggering threshold to expand CD4+ CD25+ FOXP3+ Tregs that inhibit experimental autoimmune encephalomyelitis (EAE)

المؤلفون: Moorman, Cody D., Bastian, Alexander G., DeOca, Kayla B., Mannie, Mark D.

المساهمون: National Institute of Neurological Disorders and Stroke, National Institute of Allergy and Infectious Diseases, National Institutes of Health

المصدر: Journal of Neuroinflammation ; volume 17, issue 1 ; ISSN 1742-2094

الاتاحة: http://dx.doi.org/10.1186/s12974-020-01856-8
https://link.springer.com/content/pdf/10.1186/s12974-020-01856-8.pdf
https://link.springer.com/article/10.1186/s12974-020-01856-8/fulltext.html

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4

Academic Journal

Low-Zone IL-2 Signaling: Fusion Proteins Containing Linked CD25 and IL-2 Domains Sustain Tolerogenic Vaccination in vivo and Promote Dominance of FOXP3+ Tregs in vitro

المؤلفون: DeOca, Kayla B., Moorman, Cody D., Garcia, Brandon L., Mannie, Mark D.

المساهمون: National Institutes of Health

المصدر: Frontiers in Immunology ; volume 11 ; ISSN 1664-3224

الاتاحة: http://dx.doi.org/10.3389/fimmu.2020.541619
https://www.frontiersin.org/article/10.3389/fimmu.2020.541619/full

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5

Academic Journal

A GMCSF-Neuroantigen Tolerogenic Vaccine Elicits Systemic Lymphocytosis of CD4+ CD25high FOXP3+ Regulatory T Cells in Myelin-Specific TCR Transgenic Mice Contingent Upon Low-Efficiency T Cell Antigen Receptor Recognition

المؤلفون: Moorman, Cody D., Curtis, Alan D., Bastian, Alexander G., Elliott, Sarah E., Mannie, Mark D.

المساهمون: National Institutes of Health

المصدر: Frontiers in Immunology ; volume 9 ; ISSN 1664-3224

الاتاحة: http://dx.doi.org/10.3389/fimmu.2018.03119
https://www.frontiersin.org/article/10.3389/fimmu.2018.03119/full

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6

Academic Journal

Partial CD25 Antagonism Enables Dominance of Antigen-Inducible CD25high FOXP3+ Regulatory T Cells As a Basis for a Regulatory T Cell-Based Adoptive Immunotherapy

المؤلفون: Wilkinson, Daniel S., Ghosh, Debjani, Nickle, Rebecca A., Moorman, Cody D., Mannie, Mark D.

المساهمون: National Institutes of Health

المصدر: Frontiers in Immunology ; volume 8 ; ISSN 1664-3224

الاتاحة: http://dx.doi.org/10.3389/fimmu.2017.01782
http://journal.frontiersin.org/article/10.3389/fimmu.2017.01782/full

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7

Academic Journal

IFN-β Facilitates Neuroantigen-Dependent Induction of CD25+ FOXP3+ Regulatory T Cells That Suppress Experimental Autoimmune Encephalomyelitis

المؤلفون: Wang, Duncheng, Ghosh, Debjani, Islam, S. M. Touhidul, Moorman, Cody D., Thomason, Ashton E., Wilkinson, Daniel S., Mannie, Mark D.

المصدر: The Journal of Immunology ; volume 197, issue 8, page 2992-3007 ; ISSN 0022-1767 1550-6606

الاتاحة: https://doi.org/10.4049/jimmunol.1500411
https://journals.aai.org/jimmunol/article-pdf/197/8/2992/1421046/1500411.pdf

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8

Academic Journal

Low-Zone IL-2 Signaling: Fusion Proteins Containing Linked CD25 and IL-2 Domains Sustain Tolerogenic Vaccination in vivo and Promote Dominance of FOXP3⁺ Tregs in vitro.

المؤلفون: DeOca, Kayla B., Moorman, Cody D., Garcia, Brandon L., Mannie, Mark D.

المصدر: Frontiers in Immunology; 9/23/2020, Vol. 11, pN.PAG-N.PAG, 24p

مصطلحات موضوعية: SUPPRESSOR cells, CHIMERIC proteins, MYELIN oligodendrocyte glycoprotein, T cells, TREATMENT effectiveness, T cell receptors, BCG vaccines

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9

Academic Journal

A GM-CSF-neuroantigen tolerogenic vaccine elicits inefficient antigen recognition events below the CD40L triggering threshold to expand CD4⁺ CD25⁺ FOXP3⁺ Tregs that inhibit experimental autoimmune encephalomyelitis (EAE).

المؤلفون: Moorman, Cody D., Bastian, Alexander G., DeOca, Kayla B., Mannie, Mark D.

المصدر: Journal of Neuroinflammation; 6/10/2020, Vol. 17 Issue 1, p1-19, 19p

مصطلحات موضوعية: IMMUNE recognition, SUPPRESSOR cells, MYELIN oligodendrocyte glycoprotein, T cell receptors, BACTERIAL vaccines, ENCEPHALOMYELITIS, VACCINES, IMMUNOLOGICAL tolerance, GRANULOCYTE-macrophage colony-stimulating factor, DEMYELINATION, ANIMAL experimentation, IMMUNOLOGY technique, MEMBRANE glycoproteins, GLYCOPROTEINS, RESEARCH funding, T cells, MICE, ANIMALS, ANTIGENS

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10

Academic Journal

Partial CD25 antagonism enables Dominance of antigen-inducible CD25^high FOXP3+ regulatory T cells as a Basis for a regulatory T cell- Based adoptive immunotherapy.

المؤلفون: Wilkinson, Daniel S., Ghosh, Debjani, Nickle, Rebecca A., Moorman, Cody D., Mannie, Mark D.

المصدر: Frontiers in Immunology; 12/14/2017, p1-21, 21p

مصطلحات موضوعية: CD25 antigen, FORKHEAD transcription factors, IMMUNOTHERAPY

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11

Partial cD25 antagonism enables Dominance of antigen-inducible cD25high FOXP3+ regulatory T cells as a Basis for a regulatory T cell- Based adoptive immunotherapy

المؤلفون: NC DOCKS at East Carolina University, Wilkinson, Daniel S.,Ghosh,Debjani,Nickle,Rebecca A.,Moorman,Cody D.

الاتاحة: http://libres.uncg.edu/ir/ecu/f/0000-embargo-holder.txt

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12

Academic Journal

Tolerogenic vaccines: Targeting the antigenic and cytokine niches of FOXP3+ regulatory T cells.

المؤلفون: Mannie, Mark D.¹ (AUTHOR) manniem@ecu.edu, DeOca, Kayla B.¹ (AUTHOR), Bastian, Alexander G.¹ (AUTHOR), Moorman, Cody D.¹ (AUTHOR)

المصدر: Cellular Immunology. Sep2020, Vol. 355, pN.PAG-N.PAG. 1p.

مصطلحات موضوعية: *SUPPRESSOR cells, *T cell receptors, *T cells, *MOLECULAR mimicry, *IMMUNE recognition

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