Hotchkiss et al. (2001)
|
27 sepsis patients 8, non-sepsis patients |
postmortem |
Splenic B cells were reduced in patients with sepsis, and the loss of B cells was more severe with a prolonged course of sepsis |
Hotchkiss et al. (2001)
|
Holub et al. (2003)
|
32 sepsis patients 34 healthy controls |
Day 1, 3, 7, and 14 after admission |
B-cell counts were not changed in sepsis patients, but decreased B-cell counts on days 3 and 7 were associated with nosocomial infections |
Holub et al. (2003)
|
Gogos et al. (2010)
|
505 sepsis patients |
Within 24 h after diagnosis |
Absolute B-cell counts were lower in patients with severe sepsis/shock compared to sepsis; B-cell counts within 24 h of diagnosis in patients correlate with infectious pathogens |
Gogos et al. (2010)
|
Venet et al. (2010)
|
21 septic shock patients |
Within 2 h after diagnosis and the next 48 h |
B-cell numbers were reduced within 48 h |
Venet et al. (2010)
|
Andaluz-Ojeda et al. (2011)
|
50 patients with severe sepsis or septic shock |
Day 1, 3, and 10 after admission |
Non-survivors had decreased B cell numbers on both days 3 and 7, but not significantly compared with survivors |
Andaluz-Ojeda et al. (2011)
|
Monserrat et al. (2013)
|
52 septic shock patients 36 healthy controls |
On the day of admission and 3, 7, 14, and 28 days later |
The counts of CD23+ B cells and CD5+ B cells were reduced, while the proportion of CD23+ B cells and CD69+ B cells is increased at ICU admission. The absolute counts of CD40+ B cells were decreased and the percentages of CD95+ and CD80+ B cells were increased in non-surviving patients |
Monserrat et al. (2013)
|
Suzuki et al. (2016)
|
33 severe sepsis patients, 44 healthy controls |
Within 72 h after diagnosis and at 8–11 days later |
Naive B-cell populations were reduced in chronic sepsis patients compared with HCs and acute sepsis patients; the percentage of CD21-/low B cells was increased in sepsis patients |
Suzuki et al. (2016)
|
Shankar-Hari et al. (2017a)
|
101 sepsis patients |
On the day of admission |
The proportions of plasmablasts, IgM memory B cells, and class-switched memory B cells were reduced; B-cell apoptosis was highest in the memory subsets |
Shankar-Hari et al. (2017a)
|
Gustave et al. (2018)
|
138 septic shock patients 48 healthy controls |
Day 1, 2, and 6 after diagnosis |
B-cell counts decreased but the percentage increased; a strong decrease in HLA-DR expression appeared on day 1 and persisted through day 6; the proportion of CD21low CD95high B cells was increased |
Gustave et al. (2018)
|
Wilson et al. (2018)
|
22 sepsis patients 11 healthy controls |
Within 12 h of ICU admission |
Higher percentages of PD-1 and PD-L1 in CD27+ and CD27− B cells and higher percentages of PD-L2 in CD27+ B cells in sepsis |
Wilson et al. (2018)
|
Brinkhoff et al. (2019)
|
20 healthy volunteers (LPS or placebo injection) |
Up to 72 h after injection |
At 3 h after LPS injection, the absolute numbers of B cells decreased, while the relative proportions of naive B cells and plasmablasts increased, and the percentage of memory B cells decreased |
Brinkhoff et al. (2019)
|
Dong et al. (2020)
|
33 septic shock patients 10 healthy controls |
Day 1, 3, and 7 |
Patients with septic shock had lower immature transitional (IM) B cells and resting memory (RM) B cell counts, higher percentages of tissue-like memory B and activated memory B cells, and lower percentages of IM B and RM B cells |
Dong et al. (2020)
|
Duan et al. (2020)
|
40 sepsis patients |
Within 24 h of the onset and 24 h later |
Non-survivors had lower numbers of B and Tfh cells, and the main difference in subpopulations was not naive B cells, but mature B cells |
Duan et al. (2020)
|