Lineage tracing of human B cells reveals the in vivo landscape of human antibody class switching

Author:

Horns Felix1ORCID,Vollmers Christopher23,Croote Derek2ORCID,Mackey Sally F4,Swan Gary E56,Dekker Cornelia L4,Davis Mark M78,Quake Stephen R2910

Affiliation:

1. Biophysics Graduate Program, Stanford University, Stanford, United States

2. Department of Bioengineering, Stanford University, Stanford, United States

3. Department of Biomolecular Engineering, University of California Santa Cruz, Santa Cruz, United States

4. Department of Pediatrics, Stanford University School of Medicine, Stanford, United States

5. Stanford Prevention Research Center, Stanford University School of Medicine, Stanford, United States

6. Department of Medicine, Stanford University School of Medicine, Stanford, United States

7. Department of Microbiology and Immunology, Stanford University School of Medicine, Stanford, United States

8. Institute of Immunity, Transplantation and Infection, Stanford University School of Medicine, Stanford, United States

9. Department of Applied Physics, Stanford University, Stanford, United States

10. Howard Hughes Medical Institute, Chevy Chase, United States

Abstract

Antibody class switching is a feature of the adaptive immune system which enables diversification of the effector properties of antibodies. Even though class switching is essential for mounting a protective response to pathogens, the in vivo patterns and lineage characteristics of antibody class switching have remained uncharacterized in living humans. Here we comprehensively measured the landscape of antibody class switching in human adult twins using antibody repertoire sequencing. The map identifies how antibodies of every class are created and delineates a two-tiered hierarchy of class switch pathways. Using somatic hypermutations as a molecular clock, we discovered that closely related B cells often switch to the same class, but lose coherence as somatic mutations accumulate. Such correlations between closely related cells exist when purified B cells class switch in vitro, suggesting that class switch recombination is directed toward specific isotypes by a cell-autonomous imprinted state.

Funder

National Science Foundation

National Institutes of Health

Publisher

eLife Sciences Publications, Ltd

Subject

General Immunology and Microbiology,General Biochemistry, Genetics and Molecular Biology,General Medicine,General Neuroscience

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