A photo of Jack Bleesing.

Jacob "Jack" J.H. Bleesing, MD, PhD


  • Co-Director, Diagnostic Immunology Laboratories
  • Associate Director, Immunodeficiency and Histiocytosis Program
  • Professor, UC Department of Pediatrics

About

MD: University of Leiden, Leiden, The Netherlands, 1989.

PhD: University of Leiden, Leiden, The Netherlands, 2002.

Residency: Pediatrics, University of Florida, Gainesville, Florida, 1993.

Fellowship: Allergy/Immunology, Duke University Medical Center, Durham, North Carolina, 1995.

Fellowship: Clinical Laboratory Immunology, National Institutes of Health, Bethesda, Maryland, 2001.

Interests

Immunobiology; translational research; immunologic methods development

Services and Specialties

Cancer and Blood Diseases, Immune Deficiencies and Histiocytosis, Bone Marrow Transplantation BMT, Leukemia, Hemophagocytic lymphohistiocytosisHLH, Rare Lung Diseases

Interests

Clinical investigation of primary immunodeficiency disorders (with emphasis on disorders of immuno dysregulation and B-cell disorders); immuno-reconstitution following blood and marrow transplantation; diagnostic immunology (with emphasis on flow cytometry)

Additional Languages

Dutch, German

Insurance Information

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Publications

Genetic Testing in Patients with Autoimmune Lymphoproliferative Syndrome: Experience of 802 Patients at Cincinnati Children's Hospital Medical Center. Xu, X; Denton, J; Wu, Y; Liu, J; Guan, Q; Dawson, DB; Bleesing, J; Zhang, W. Journal of Clinical Immunology. 2024; 44:166.

COVID-19 Vaccination in Patients with Inborn Errors of Immunity Reduces Hospitalization and Critical Care Needs Related to COVID-19: a USIDNET Report. McDonnell, J; Cousins, K; Younger, ME M; Lane, A; Abolhassani, H; Abraham, RS; Al-Tamemi, S; Aldave-Becerra, JC; Al-Faris, EH; Alfaro-Murillo, A; Lim, XR; Lopes, JP; López, AL; Tarquini, L. Journal of Clinical Immunology. 2024; 44:86.

68 LRBA dysfunction: a new diagnostic entity caused by biallelic LRBA missense variants results in reduced CTLA-4 expression and autoimmunity. Chiang, S; Murguia-Favela, L; Wright, N; Steele, M; Seroogy, C; Blanchard-Rohner, G; Shrikhande, A; Wilson, J; Yang, L; Owsley, E; Derfalvi, B; Brager, R; Jordan, M; Marwaha, A. Clinical Immunology. 2024; 262:110010.

Allogeneic hematopoietic cell transplantation is effective for p47phox chronic granulomatous disease: A  Primary Immune Deficiency Treatment Consortium study. Grunebaum, E; Arnold, DE; Logan, B; Parikh, S; Marsh, RA; Griffith, LM; Mallhi, K; Chellapandian, D; Lim, SS; Deal, CL; Torgerson, TR; Malech, HL; Kang, EM; Leiding, JW. Journal of Allergy and Clinical Immunology. 2024; 153:1423-1431.e2.

Clinical, immunological features, treatments, and outcomes of autoimmune hemolytic anemia in patients with RAG deficiency. Wang, C; Sun, B; Wu, K; Farmer, JR; Ujhazi, B; Geier, CB; Gordon, S; Westermann-Clark, E; Savic, S; Secord, E; Wang, W; Wang, JY; Wang, X; Walter, JE. Blood Advances. 2024; 8:603-607.

Posttransplantation late complications increase over time for patients with SCID: A Primary Immune Deficiency Treatment Consortium (PIDTC) landmark study. Eissa, H; Thakar, MS; Shah, AJ; Logan, BR; Griffith, LM; Dong, H; Parrott, RE; O'Reilly, RJ; Dara, J; Kapoor, N; Haddad, E; Buckley, RH; Cowan, MJ; Heimall, J. Journal of Allergy and Clinical Immunology. 2024; 153:287-296.

Genotype, oxidase status, and preceding infection or autoinflammation do not affect allogeneic HCT outcomes for CGD. Leiding, JW; Arnold, DE; Parikh, S; Logan, B; Marsh, RA; Griffith, LM; Wu, R; Kidd, S; Mallhi, K; Chellapandian, D; Pulsipher, MA; Torgerson, TR; Malech, HL; Kang, EM. Blood. 2023; 142:2105-2118.

Clinical Characteristics, Management, and Allogeneic Hematopoietic Cell Transplantation of Patients with Toll-like Receptor 8 Gain-of-Function Mutations. Arnold, DE; Kaviany, S; Aluri, J; Murguia-Favela, L; Wright, NA; Loughran, TP; Powell, J; De Ravin, SS; Rao, VK; Holland, S; Bleesing, J; Bednarski, JJ; Connelly, JA; Cooper, M. Blood. 2023; 142:936.

Measuring the effect of newborn screening on survival after haematopoietic cell transplantation for severe combined immunodeficiency: a 36-year longitudinal study from the Primary Immune Deficiency Treatment Consortium. Thakar, MS; Logan, BR; Puck, JM; Dunn, EA; Buckley, RH; Cowan, MJ; O'Reilly, RJ; Kapoor, N; Satter, LF; Pai, SY; Griffith, LM; Haddad, E; Dvorak, CC; Notarangelo, LD. The Lancet. 2023; 402:129-140.

Autoimmune Lymphoproliferative Syndrome (ALPS) Disease and ALPS Phenotype: Are They Two Distinct Entities?. Palmisani, E; Miano, M; Grossi, A; Lanciotti, M; Lupia, M; Terranova, P; Ceccherini, I; Montanari, E; Calvillo, M; Pierri, F; Crescenzio, N; Bleesing, J; Dufour, C; Fioredda, F. HemaSphere. 2023; 7:e845.

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