Two Distinct Durable Human Class-switched Memory B Cell Populations Are Induced by Vaccination and Infection.
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April 2025
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Available in CDC Stacks on January 21, 2026, 12:00 AM
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Alternative Title:Cell Reports, 2025, v. 44, no. 4: Two Distinct Durable Human Class-switched Memory B Cell Populations Are Induced by Vaccination and Infection.
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Journal Article:Cell Reports
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Personal Author:Perugino, Cory A. ; Liu, Hang ; Feldman, Jared ; Marbourg, Jess ; Guy, Thomas V. ; Hui, Anson ; Ingram, Nicole ; Liebaert, Julian ; Chaudhary, Neha ; Tao, Weiyang ; Jacob-Dolan, Catherine ; Hauser, Blake M. ; Mian, Zayd ; Nathan, Anusha ; Zhao, Zezhou ; Kaseke, Clarety ; Tano-Menka, Rhoda ; Getz, Matthew A. ; Senjobe, Fernando ; Berrios, Cristhian ; Ofoman, Onosereme ; Manickas-Hill, Zachary ; Wesemann, Duane R. ; Lemieux, Jacob E. ; Goldberg, Marcia B. ; Nündel, Kerstin ; Moormann, Ann ; Marshak-Rothstein, Ann ; Larocque, Regina C. ; Ryan, Edward T. ; Iafrate, John A. ; Lingwood, Daniel ; Gaiha, Gaurav ; Charles, Richelle ; Balazs, Alejandro B. ; Pandit, Aridaman ; Naranbhai, Vivek ; Schmidt, Aaaron G. ; Pillai, Shiv
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Description:Memory lymphocytes are durable cells that persist in the absence of antigen, but few human B cell subsets have been characterized in terms of durability. The relative durability of eight non-overlapping human B cell sub-populations covering 100% of all human class-switched B cells was interrogated. Only two long-lived B cell populations persisted in the relative absence of antigen. In addition to canonical germinal center-derived switched-memory B cells with an IgD
CD27
CXCR5
phenotype, a second, non-canonical, but distinct memory population of IgD
CD27
CXCR5
DN1 B cells was also durable, exhibited a unique TP63-linked transcriptional and anti-apoptotic signature, had low levels of somatic hypermutation, but was more clonally expanded than canonical switched-memory B cells. DN1 B cells likely evolved to preserve immunological breadth and may represent the human counterparts of rodent extrafollicular memory B cells that, unlike canonical memory B cells, can enter germinal centers and facilitate B cell and antibody evolution. -
Content Notes:Author manuscript
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Source:Cell Reports, 2025, v. 44, no. 4
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DOI:
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ISSN:2211-1247
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Pubmed ID:40173042
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Pubmed Central ID:PMC12820432
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Document Type:
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Funding:R01 AI153098/AI/NIAID NIH HHSUnited States/ ; R01 AI155447/AI/NIAID NIH HHSUnited States/ ; U19 AI110495/AI/NIAID NIH HHSUnited States/ ; R01 AI146785/AI/NIAID NIH HHSUnited States/ ; U01 CK000490/CK/NCEZID CDC HHSUnited States/ ; T32 GM144273/GM/NIGMS NIH HHSUnited States/ ; U01 CK000633/CK/NCEZID CDC HHSUnited States/
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Genre:
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Pages in Document:115472 (27 pdf pages)
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Volume:44
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Issue:4
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Main Document Checksum:urn:sha-512:22701fa8327b17b97d9e70638dc49cdf10241c3f15dab52a925070845390941ef3149360cad6bf02e1561a7575d12c047616dd615ac498841fbd6b10663da04d
Supporting Files
File Language:
English
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