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Profil bibliographique

Brian Groff

Informations fournies par OpenAlex. Research Africa ne déduit ni nationalité, ni poste, ni coordonnées personnelles.

44Publications signalées
477Citations signalées
1Affiliations récentes

Les institutions déclarées

Les domaines associés

CAR-T cell therapy researchImmune Cell Function and InteractionCRISPR and Genetic EngineeringPluripotent Stem Cells ResearchImmunotherapy and Immune Responses

Les publications récentes

2026 conference-abstract OpenAlex

Abstract 4284: FT839: A next-generation, off-the-shelf CAR T cell uniquely engineered with a dual CAR system targeting CD19 and CD38 for the treatment of hematological malignancies and autoimmune diseases without conditioning chemotherapy

Alex Garcia, Shilpi Chandra, Soheila Shirinbak, Mark Jelcic et autres

Abstract Autologous chimeric antigen receptor (CAR) T cell therapies have revolutionized treatment of hematological malignancies and are showing promising results in autoimmune settings. Despite these successes, widespread accessibility to autologous CAR T-cell therapy is challenged by manufacturing complexities, high cost, lack of …

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0 citations Cancer Research
2025 conference-abstract OpenAlex

Targeting of tumor antigen CD38 and stress antigens MICA/B by CAR T cells provides a unique approach for the comprehensive treatment of multiple myeloma

Soheila Shirinbak, Shilpi Chandra, Brian Groff, Samad Ibitokou et autres

Abstract Introduction: Recently approved autologous chimeric antigen receptor (CAR) T-cell therapies (Abecma® and Carvykti®) have demonstrated clear clinical benefit for patients with relapsed/refractory multiple myeloma (MM) with initial response rates ranging between 73-98%. Unfortunately, many of these patients ultimately relapse, often as …

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0 citations Blood
Accès ouvert 2025 conference-abstract OpenAlex

The development of FT839: An off-the-shelf CD19xCD38 dual-CAR T cell for the treatment of multiple myeloma

Spas Markov, John Reiser, Brian Groff, Shilpi Chandra et autres

Abstract Following autologous chimeric antigen receptor (CAR) T-cell therapy, approximately 50% of multiple myeloma (MM) patients relapse within two years of treatment. Relapses can occur for many reasons, but ultimately it is the result of tumor re-growth caused by the underlying attribute …

us, no, se (code pays fourni par la source)

0 citations Blood
Accès ouvert 2025 conference-abstract OpenAlex

Development of next generation multi-antigen targeting off-the-shelf CAR T cells for conditioning-free treatment of B-cell lymphoma

Shilpi Chandra, John Reiser, Brian Groff, Carissa Dege et autres

Abstract Autologous chimeric antigen receptor (CAR) T-cell therapy has had tremendous success in the treatment of hematological malignancies, yet its clinical application remains hindered by several significant limitations. Major challenges include the high cost, complex manufacturing process, the requirement for intense lymphodepleting …

us, se (code pays fourni par la source)

0 citations Blood
2025 conference-abstract OpenAlex

The development of an off-the-shelf CAR T-cell therapy co-targeting CD19 and CD38 for broad application in autoimmune disease

Mark Jelcic, Daniel Morales-Mantilla, John Reiser, Brian Groff et autres

Abstract CD19-targeting chimeric antigen receptor (CAR) T-cell therapies have demonstrated profound clinical efficacy in the treatment of a growing list of autoimmune diseases through their ability to target and reset pathogenic B cell immune compartments. The extension of CAR T-cell therapy to …

us, no, se (code pays fourni par la source)

0 citations Blood
Accès ouvert 2025 conference-abstract OpenAlex

264 Next-generation off-the-shelf CAR T cell targeting pan-tumor antigen MICA/B and engineered with immune evasion enables treatment across solid tumors without the need for conditioning chemotherapy

Eigen Peralta, Bi-Huei Yang, Shilpi Chandra, Alan M Williams et autres

Background Successful implementation of chimeric antigen receptor (CAR) T-cell therapies in solid tumors faces multiple obstacles, including challenges in selecting appropriate tumor antigens and ensuring consistent and scaled product manufacturing for on-demand patient treatment. Moreover, both autologous and allogeneic CAR T-cell therapies …

us, no, se (code pays fourni par la source)

0 citations Regular and Young Investigator Award Abstracts
Accès ouvert 2025 preprint OpenAlex

Toggling of NKG2A expression drives functional specialization of iPSC-derived CAR NK cells

Minoru Kanaya, Camille Philippon, Herman Netskar, Michelle Sætersmoen et autres

Induced pluripotent stem cell (iPSC)-derived natural killer (iNK) cells offer a promising platform for off-the-shelf immunotherapy against hematological malignancies. NK cell function is dynamically regulated through education driven by inhibitory receptors, including CD94/NKG2A and killer cell immunoglobulin-like receptors (KIR). However, the acquisition …

no, se, us (code pays fourni par la source)

2 citations bioRxiv (Cold Spring Harbor Laboratory)
Accès ouvert 2024 conference-abstract OpenAlex

Alloimmune Defense Receptor Combined with Genetic Ablation of Adhesion Ligand CD58 Is a Comprehensive Approach to Promote Functional Persistence of Allogeneic Cell Therapies without Conditioning Chemotherapy

Alan M Williams, Rina M. Mbofung, Daniel Morales-Mantilla, Brian Groff et autres

Clinical administration of chimeric antigen receptor (CAR) T cell and CAR NK cell therapies rely on conditioning chemotherapy (CCT) to deplete the host immune system, maximize access to homeostatic cytokines, and promote cell expansion and functional persistence. However, CCT also elicits pan-immune …

us, se (code pays fourni par la source)

2 citations Blood
Accès ouvert 2024 conference-abstract OpenAlex

336 Alloimmune defense receptor with genetic ablation of adhesion ligand CD58 promotes functional persistence of allogeneic cell therapies without conditioning chemotherapy

Alan M Williams, Rina M. Mbofung, Daniel Morales-Mantilla, Brian Groff et autres

Background Clinical administration of chimeric antigen receptor (CAR) NK cell and CAR T-cell therapies require conditioning chemotherapy (CCT) to deplete the host immune system, maximize access to homeostatic cytokines, and promote cell expansion and functional persistence. However, CCT also elicits pan-immune cell …

us, se (code pays fourni par la source)

0 citations Regular and Young Investigator Award Abstracts
Accès ouvert 2024 article OpenAlex

Genetic ablation of adhesion ligands mitigates rejection of allogeneic cellular immunotherapies

Quirin Hammer, Karlo Perica, Rina M. Mbofung, Hanna van Ooijen et autres

Allogeneic cellular immunotherapies hold promise for broad clinical implementation but face limitations due to potential rejection of donor cells by the host immune system. Silencing of beta-2 microglobulin (B2M) expression is commonly employed to evade T cell-mediated rejection by the host, although …

se, us, no (code pays fourni par la source)

40 citations Cell stem cell
2024 conference-abstract OpenAlex

Abstract 3618: High-avidity BCMA CAR and high-affinity, non-cleavable CD16 Fc receptor incorporated in off-the-shelf CAR T cells promote multi-antigen targeting and durable anti-tumor cytotoxicity in the treatment of multiple myeloma

John Reiser, Alison O’Connor, Bryan Hancock, Spas Markov et autres

Abstract Immune cell therapy has proven highly effective for the treatment of multiple myeloma (MM). However, key challenges remain that include disease relapse, limited patient access, and inability to effectively combine with existing standard-of-care therapies. Rapid progress in the development of off-the-shelf, …

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1 citation Cancer Research
Accès ouvert 2023 preprint OpenAlex

Genetic ablation of adhesion ligands averts rejection of allogeneic immune cells

Quirin Hammer, Karlo Perica, Hanna van Ooijen, Rina M. Mbofung et autres

SUMMARY Allogeneic cell therapies hold promise for broad clinical implementation, but face limitations due to potential rejection by the recipient immune system. Silencing of beta-2-microglobulin ( B2M ) expression is commonly employed to evade T cell-mediated rejection, although absence of B2M triggers …

se, us, no (code pays fourni par la source)

7 citations bioRxiv (Cold Spring Harbor Laboratory)

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