Abstract
Objective
To delineate disturbances in peripheral B cell memory in primary Sjögren's syndrome (SS).
Methods
Isotype‐specific immunoglobulin (Ig) heavy‐chain transcripts were analyzed in single‐sorted CD19+,CD27− naive and CD19+,CD27+ memory B cells from patients with primary SS and normal healthy control subjects.
Results
A significantly higher frequency of B cells expressing μ‐, α‐, and/or γ‐chain transcripts were found in patients with primary SS compared with controls (58.0% versus 14.3%; P < 0.0001). Notably, 30.5% of individual B cells (for primary SS, 38.7%; for controls, 12.7% [P < 0.0001]) simultaneously expressed transcripts for different Ig heavy‐chain isotypes using identical V~H~–D–J~H~ rearrangements. However, these cells lacked surface expression of more than one of the respective Ig heavy‐chain isotypes as well as messenger RNA (mRNA) transcripts for 2 germinal center markers, activation‐induced cytidine deaminase, and Bcl‐6. In contrast with the findings in normal healthy controls, peripheral B cell memory in patients with primary SS was characterized by 1) circulating CD27+ B cells expressing heavily mutated Ig V~H~ transcripts (mutational frequency 8.6% versus 4.3%; P < 0.0001), 2) significantly enhanced mutational frequencies of Cμ transcripts (9.6% versus 2.5%; P < 0.0001), 3) a high proportion (61.2%) of CD27+ B cells expressing transcripts for multiple Ig heavy‐chain isotypes, and 4) a CD27− memory‐type B cell subpopulation expressing mutated Cμ transcripts.
Conclusion
Altogether, both B cell hyperactivity and striking abnormalities in peripheral B cell memory are indicated at the single‐cell mRNA level in patients with primary SS. Detection of multiple Ig heavy‐chain transcripts in peripheral CD19+,CD27+ memory B cells of patients with SS may represent the abnormal retention of pre‐switch mRNA transcripts in circulating post‐switch B cells.