David H. McKenna
Current Organizations / Institutes
The organizations/institutes from the scholar's latest article
Previous Organizations / Institutes
The organizations / institutes from the scholar's other articles in the past ten years
Research Subjects
David H. McKenna has a total of 403 co-authors. Here are the top co-authors by number of shared publications:
Darin Sumstad
10 shared publications- Marcelo Pasquini
Medical College of Wisconsin, Milwaukee, USA
10 shared publications - Aaron P. Rapoport
Division of Hematology/Oncology, University of Maryland Greenebaum Comprehensive Cancer Center, Baltimore, MD
9 shared publications - Adam Mendizabal
26Emmes, Rockville, MD
9 shared publications - Ajay K. Nooka
Winship Cancer Institute, Emory University, Atlanta, USA
9 shared publications - Alan Howard
Medical College of Wisconsin, Milwaukee, Wisconsin
9 shared publications
Latest Publications
- 24 September 2026
- Published by Wiley in Transfusion
- Vol. 66 (11) , 2335-2347
Global evaluation of cellular therapy processing facility medical director and laboratory director training: The BEST collaborative study
Background: Cell processing facility accreditation requires Medical Directors and Laboratory Directors, but formal training pathways are not systematically delineated. This study provides information on cell processing facility Medical Directors and Laboratory Directors' role‐specific education (RSE) worldwide. Study Design and Methods: Data collected on cell processing facilities included country, staff, regulatory and accreditation status, institutional affiliation, cellular therapy product types, and volume. Questions regarding Medical Directors included country, clinical specialty and subspecialty, year completed, and formal RSE. Laboratory Director questions included country and training focus, year completed, and formal RSE. Results: Surveys completed ( n = 123) included Medical Directors ( n = 70) and Laboratory Directors ( n = 71) across 30 countries over 6 continents. Medical Directors reported 101 clinical specialties, and 72 clinical subspecialties, of which 34 (33.3%) and 39 (54.2%) included RSE, respectively. Laboratory Directors ( n = 71) held MD ( n = 20), PhD ( n = 34), MD/PhD ( n = 7), or other ( n = 11) academic degrees. Laboratory Directors with MDs completed 42 clinical specialties and 27 clinical subspecialties, 15 (35.8%) and 13 (48.1%) of which included RSE, respectively. Six of 52 (11.5%) Laboratory Directors with graduate or other academic degrees ( n = 52) included RSE. Role‐specific educational experiences varied highly across all training programs. Notably, most responses for any given role and educational activity indicated no experience at all. Discussion: Standardized role‐specific educational programs for cell processing facility Medical Directors and Laboratory Directors are lacking and, when present, are highly variable. Coordinated development of educational content and reciprocally acknowledged curricula and certificates could help standardize training for future cell processing facility leaders.
- 24 September 2026
- Published by Wiley in Transfusion
- Vol. 66 (11) , 2335-2347
Global evaluation of cellular therapy processing facility medical director and laboratory director training: The BEST collaborative study
Background: Cell processing facility accreditation requires Medical Directors and Laboratory Directors, but formal training pathways are not systematically delineated. This study provides information on cell processing facility Medical Directors and Laboratory Directors' role‐specific education (RSE) worldwide. Study Design and Methods: Data collected on cell processing facilities included country, staff, regulatory and accreditation status, institutional affiliation, cellular therapy product types, and volume. Questions regarding Medical Directors included country, clinical specialty and subspecialty, year completed, and formal RSE. Laboratory Director questions included country and training focus, year completed, and formal RSE. Results: Surveys completed ( n = 123) included Medical Directors ( n = 70) and Laboratory Directors ( n = 71) across 30 countries over 6 continents. Medical Directors reported 101 clinical specialties, and 72 clinical subspecialties, of which 34 (33.3%) and 39 (54.2%) included RSE, respectively. Laboratory Directors ( n = 71) held MD ( n = 20), PhD ( n = 34), MD/PhD ( n = 7), or other ( n = 11) academic degrees. Laboratory Directors with MDs completed 42 clinical specialties and 27 clinical subspecialties, 15 (35.8%) and 13 (48.1%) of which included RSE, respectively. Six of 52 (11.5%) Laboratory Directors with graduate or other academic degrees ( n = 52) included RSE. Role‐specific educational experiences varied highly across all training programs. Notably, most responses for any given role and educational activity indicated no experience at all. Discussion: Standardized role‐specific educational programs for cell processing facility Medical Directors and Laboratory Directors are lacking and, when present, are highly variable. Coordinated development of educational content and reciprocally acknowledged curricula and certificates could help standardize training for future cell processing facility leaders.
- Open Access
- 20 June 2026
- Published by Elsevier in Cytotherapy
- Vol. 28 (10)
Human mesenchymal stromal cell extracellular vesicles maintain therapeutic miRNA cargo despite exposure to cystic fibrosis bronchoalveolar lavage fluid
- 20 June 2026
- Published by Elsevier in Cytotherapy
- Vol. 28 (10)
Open AccessHuman mesenchymal stromal cell extracellular vesicles maintain therapeutic miRNA cargo despite exposure to cystic fibrosis bronchoalveolar lavage fluid
- 21 June 2025
- Published by Elsevier in Cytotherapy
- Vol. 27 (10) , 1229-1239
Clinical manufacture of CRISPR/Cas9-based cytokine-induced SH2 protein knock-out tumor-infiltrating lymphocytes for gastrointestinal cancers
- 21 June 2025
- Published by Elsevier in Cytotherapy
- Vol. 27 (10) , 1229-1239
Clinical manufacture of CRISPR/Cas9-based cytokine-induced SH2 protein knock-out tumor-infiltrating lymphocytes for gastrointestinal cancers
- Open Access
- 20 January 2025
- Published by Elsevier in Cytotherapy
- Vol. 27 (5) , 581-596
Acute respiratory distress vs healthy lung environments differently affect mesenchymal stromal cell extracellular vesicle miRNAs
- 20 January 2025
- Published by Elsevier in Cytotherapy
- Vol. 27 (5) , 581-596
Open AccessAcute respiratory distress vs healthy lung environments differently affect mesenchymal stromal cell extracellular vesicle miRNAs
- Open Access
- 16 September 2024
- Published by American Association for Cancer Research (AACR)
Study Representativeness Table1 from Randomized Trial of a Personalized Dendritic Cell Vaccine after Autologous Stem Cell Transplant for Multiple Myeloma
Study representation of underserved communities
- 16 September 2024
- Published by American Association for Cancer Research (AACR)
Open AccessStudy Representativeness Table1 from Randomized Trial of a Personalized Dendritic Cell Vaccine after Autologous Stem Cell Transplant for Multiple Myeloma
Study representation of underserved communities
- Open Access
- 16 September 2024
- Published by American Association for Cancer Research (AACR)
Figure S1 from Randomized Trial of a Personalized Dendritic Cell Vaccine after Autologous Stem Cell Transplant for Multiple Myeloma
Supplemental Figure 1: (A) Progression Free Survival Kaplan Meier Curve. (B) Overall Survival Kaplan Meier Curve.
- 16 September 2024
- Published by American Association for Cancer Research (AACR)
Open AccessFigure S1 from Randomized Trial of a Personalized Dendritic Cell Vaccine after Autologous Stem Cell Transplant for Multiple Myeloma
Supplemental Figure 1: (A) Progression Free Survival Kaplan Meier Curve. (B) Overall Survival Kaplan Meier Curve.
- Open Access
- 16 September 2024
- Published by American Association for Cancer Research (AACR)
Study Representativeness Table1 from Randomized Trial of a Personalized Dendritic Cell Vaccine after Autologous Stem Cell Transplant for Multiple Myeloma
Study representation of underserved communities
- 16 September 2024
- Published by American Association for Cancer Research (AACR)
Open AccessStudy Representativeness Table1 from Randomized Trial of a Personalized Dendritic Cell Vaccine after Autologous Stem Cell Transplant for Multiple Myeloma
Study representation of underserved communities
- Open Access
- 16 September 2024
- Published by American Association for Cancer Research (AACR)
Figure S1 from Randomized Trial of a Personalized Dendritic Cell Vaccine after Autologous Stem Cell Transplant for Multiple Myeloma
Supplemental Figure 1: (A) Progression Free Survival Kaplan Meier Curve. (B) Overall Survival Kaplan Meier Curve.
- 16 September 2024
- Published by American Association for Cancer Research (AACR)
Open AccessFigure S1 from Randomized Trial of a Personalized Dendritic Cell Vaccine after Autologous Stem Cell Transplant for Multiple Myeloma
Supplemental Figure 1: (A) Progression Free Survival Kaplan Meier Curve. (B) Overall Survival Kaplan Meier Curve.
- 30 March 2024
- Published by Elsevier in Cytotherapy
- Vol. 26 (9) , 1062-1075
Inter- and Intra-donor variability in bone marrow–derived mesenchymal stromal cells: implications for clinical applications
- 30 March 2024
- Published by Elsevier in Cytotherapy
- Vol. 26 (9) , 1062-1075
Inter- and Intra-donor variability in bone marrow–derived mesenchymal stromal cells: implications for clinical applications