HSC extrinsic sex-related and intrinsic autoimmune disease–related human B-cell variation is recapitulated in humanized mice

Author:

Borsotti Chiara1,Danzl Nichole M.1,Nauman Grace1,Hölzl Markus A.1,French Clare1,Chavez Estefania1,Khosravi-Maharlooei Mohsen1,Glauzy Salome2,Delmotte Fabien R.2,Meffre Eric2,Savage David G.3,Campbell Sean R.1,Goland Robin45,Greenberg Ellen45,Bi Jing6,Satwani Prakash7,Yang Suxiao1,Bathon Joan6,Winchester Robert6,Sykes Megan1

Affiliation:

1. Columbia Center for Translational Immunology, Department of Medicine, College of Physicians and Surgeons, Columbia University, New York, NY;

2. Department of Immunobiology, Yale University School of Medicine, New Haven, CT;

3. Division of Hematology/Oncology, Department of Medicine,

4. Department of Medicine,

5. Naomi Berrie Diabetes Center, and

6. Division of Rheumatology, Department of Medicine, College of Physicians and Surgeons, Columbia University, New York, NY; and

7. Department of Pediatrics, Columbia University, New York, NY

Abstract

Key Points Increased human B-cell reconstitution is seen in female compared to male mice in multiple humanized mouse models. The PI mouse model recapitulates HSC-intrinsic autoimmune defects from T1D and RA bone marrow donors.

Publisher

American Society of Hematology

Subject

Hematology

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