@article{oai:shiga-med.repo.nii.ac.jp:00004108,
 author = {山下, 典亮 and 今井, 隆行 and 河原, 真大 and 稲富, 理 and 安藤, 朗 and YAMASHITA, Noriaki and IMAI, Takayuki and KAWAHARA, Masahiro and INATOMI, Osamu and ANDOH, Akira},
 issue = {1},
 journal = {Journal of Clinical Biochemistry and Nutrition},
 month = {Jan},
 note = {pdf, Vedolizumab is a humanized monoclonal antibody against the α4β7 integrin and is approved for treatment of inflammatory bowel diseases. In this study, we evaluated the immunogenicity of vedolizumab using a simple drug-tolerant assay developed in our laboratory. Serum vedolizumab trough levels and anti-vedolizumab antibody (AVA) levels were measured using new immunoassays in 37 patients with ulcerative colitis (UC) under vedolizumab maintenance therapy. The median vedolizumab trough level at week 30 was 16.0 μg/ml (interquartile range, 7.3-24.4). The vedolizumab trough level of the patients with clinical remission (partial Mayo score ≤1) was significantly higher than that of clinically active patients (16.7 μg/ml vs 6.8). The cut-off value of vedolizumab level predicting clinical remission at week 30 was 7.34 μg/ml. The median AVA level of patients under vedolizumab maintenance therapy was similar to that of healthy controls (n = 20) (0.032 μg/ml-c vs 0.022). One of 37 patients (2.7%) was judged to be AVA positive. There was no significant difference in serum AVA and vedolizumab trough levels between biologics-naïve (n = 19) and biologics-switched (prior anti-TNFα-exposed) patients (n = 18). In conclusion, the simple drug-tolerant assay developed in our laboratory demonstrated low immuno-genicity of vedolizumab. Prior use of anti-TNFα drugs did not affect the immunogenicity of vedolizumab., Journal Article},
 pages = {72--78},
 title = {Low immunogenicity of vedolizumab determined by a simple drug-tolerant assay in patients with ulcerative colitis.},
 volume = {70},
 year = {2022}
}