Skip to main content
. 2022 Feb 3;13:811200. doi: 10.3389/fimmu.2022.811200

Table 2.

Summary of pathological HLA-G neoexpression in solid and hematopoietic malignancies.

Tumor Entity Cell Lines/tumor Samples/Plasma Samples; Number of Samples Method/Applied Antibody Frequency of HLA-G Expression Correlation of the HLA-G with Clinical Parameters References
breast cancer 235 primary breast cancer lesions; 44 plasma samples of breast cancer patients and 48 plasma samples of healthy controls IHC (mAb HGY), ELISA 66% HLA-G positive breast cancers; sHLA-G: 0.74 μg/mL in stage I patients, sHLA-G: 0.78 μg/mL in stage II patients; sHLA-G: 0.43 μg/mL in healthy donors statistically significant correlation tumor size (p = 0.0001), nodal status (p = 0.012), disease stage (p = 0.0001), HLA-G positive patients with lower survival rate (p < 0.028); elevated sHLA-G levels in plasma of breast cancer patients (p < 0.001) (71)
breast cancer 677 early breast cancer lesions IHC (mAb 4H84) 60% HLA-G positive breast cancers predictor for breast cancer patients (72)
cervical cancer 22 normal cervical tissues, 14 cervical intraepithelial neoplasia patients, IHC (mAb 4H84) 0% in normal cervical tissues, 35.7% in cervical intraepithelial neoplasia, 62.8% in squamous cell cervical cancer patients association with disease progression (73)
129 patients with squamous cell cervical cancer
cervical cancer 22 normal cervical tissues, 119 primary cervical lesions; IHC (mAb 4H84), 0% in normal cervical tissues, significant correlation (p < 0.05) to size of the main lesion, parametrical invasion and lymph node metastasis (74)
172 plasma samples of patients with cervical cancer and 20 plasma samples of healthy controls ELISA (MEM-G/9) 45% in primary cervical lesions;
statistically significant higher sHLA-G levels in plasma of cervical patients (median 191.4 U/ml) versus plasma of healthy controls (median 45.18 U/ml, p < 0.001)
colorectal cancer (CRC) 457 primary colorectal cancer (CRC) (colon = 232, rectal = 225 lesions) IHC (mAb 4H84) 70.7% HLA-G positive CRC specimen significant association with worse prognosis (p = 0.042) (75)
colorectal cancer 144 plasma samples of CRC patients, ELISA (MEM-G/9) statistically significant (p < 0.01) increased sHLA-G plasma levels in CRC patients (median 124.3 U/ml) than in healthy controls (median 25 U/ml) no correlation (76)
60 plasma samples of healthy controls
gastric cancer 94 unselected patients with gastric adenocarcinoma IHC (mAb, 4H84) 25.5% HLA-G positive gastric adenocarcinoma specimen significant association with (p < 0.0001), worse survival (77)
(stage I to III)
glioblastoma 108 glioblastoma specimen IHC (mAb, MEM-G/02) 60.2% HLA-G positive glioblastoma specimen negative effects on the survival rate (78)
hepatocellular carcinoma 74 primary hepatocellular carcinoma specimen IHC (mAb, 4H84) 31% HLA-G positive hepatocellular carcinoma specimen no correlation (79)
ovarian cancer 169 primary ovarian carcinoma lesions with type II, high grade serous and undifferentiated IHC (mAb 4H84) 47.9% HLA-G positive primary ovarian cancer specimen significant correlation with a favorable prognosis (80)
(p = 0.038)
ovarian cancer 33 primary ovarian carcinoma lesions, IHC (mAb 4H84) 66.7% HLA-G positive primary ovarian cancer specimen, protection from NK cell lysis (81)
13 normal ovarian tissues 0% of the normal ovarian tissues (in vitro)
pancreatic carcinoma 42 primary pancreatic carcinoma specimen IHC (mAb, 4H84) 66% HLA-G positive pancreatic carcinoma specimen significant correlation with grade (p=0.007), stage (p=0.038) and poor prognosis (79)
testicular cancer 34 primary testicular cancer patients IHC (mAb 4H84) 20.6% HLA-G positive samples no correlation (82)
chronic 68 chronic myeloid leukemia ELISA (sHLA-G1, HLA-G5) association of sHLA-G with HLA-G alleles reduced event free survival (83)
myeloid
leukemia
chronic lymphocytic leukemia 45 chronic lymphocytic leukemia flow cytometry (MEM-G/9) 1 – 12% positive independent prognostic factor (84)