From: Roles and mechanisms of tumour-infiltrating B cells in human cancer: a new force in immunotherapy
Cancer type | ICI | Number of patients | Changes in B cells in the TME of responders | Other increasing biomarkers | Reference |
---|---|---|---|---|---|
Melanoma | Nivolumab, Ipilimumab | 41 | High proportion of class-switched memory B cells, activated B cells and GC-like B cells | BCR types, B-cell RNA signatures | [75] |
Melanoma | Nivolumab, Ipilimumab | 64 | Higher memory B cells and naive B cells | Clonal BCR repertoire, IgG | [96] |
RCC | Nivolumab, Ipilimumab | 59 | Higher plasma cells | IgG | [46] |
NSCLC | Atezolizumab | 344 | Higher B cells and plasma cells | TLSs | [85] |
NSCLC | Anti-PD-1 treatment | 12 | CD20+CD22+ADAM28+ B cells in TLSs | - | [100] |
NSCLC | Nivolumab | 150 | - | IgM+ memory B cells in peripheral blood | [99] |
Cervical cancer | Anti-PD-1 treatment | 8 | Higher B cells | Higher expression of PD-L1 | [97] |
HCC | Cabozantinib combined with Nivolumab | 15 | Higher B cells, CD138+ B cells | Higher TNF-α expression and TLSs | [98] |
SCC (Mouse model) | Anti-PD-L1 treatment | - | B cells | IgM, IgG | [101] |
BC (Mouse model) | Anti-PD-1 and CTLA-4 treatment | - | Class-switched plasma cells | IgG | [93] |