Association of CD4-positive cell infiltration with response to vedolizumab in patients with ulcerative colitis

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作者
Haruka Miyazaki
Namiko Hoshi
Tsukasa Ishida
Chiharu Nishioka
Sachiko Ouchi
Daisuke Shirasaka
Tomoo Yoshie
Yoshinori Munetomo
Yoshio Sakamoto
Tatsuya Osuga
Saori Matsui
Toshiki Hyodo
Tamami Denda
Daisuke Watanabe
Makoto Ooi
Yuzo Kodama
机构
[1] Kobe University Graduate School of Medicine,Division of Gastroenterology, Department of Internal Medicine
[2] Akashi Medical Center,Division of Gastroenterology
[3] Konan Medical Center,Division of Gastroenterology
[4] Hyogo Prefectural Harima-Himeji General Medical Center,Division of General Internal Medicine
[5] Japanese Red Cross Kobe Hospital,Division of Gastroenterology
[6] Kita-Harima Medical Center,Division of Gastroenterology
[7] Himeji Central Hospital,Division of General Surgery
[8] Hyogo Prefectural Kakogawa Medical Center,Division of Gastroenterology
[9] Takatsuki General Hospital,Division of Gastroenterology
[10] Yodogawa Christian Hospital,Division of Gastroenterology
[11] Kobe University Graduate School of Medicine,Department of Diagnostic Pathology
[12] The University of Tokyo,Department of Pathology, The Institute of Medical Science Research Hospital
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Not all patients with ulcerative colitis (UC) respond initially to treatment with biologic agents, and predicting their efficacy prior to treatment is difficult. Vedolizumab, a humanized monoclonal antibody against alpha 4 beta 7 (α4β7) integrin, suppresses immune cell migration by blocking the interaction between α4β7 integrin and mucosal addressin cell adhesion molecule 1. Reports about histological features that predict vedolizumab efficacy are scarce. So, we examined the association between histological features and vedolizumab efficacy. This was a multicenter, retrospective study of patients with UC treated with vedolizumab. Biopsy specimens taken from the colonic mucosa prior to vedolizumab induction were used, and the areas positively stained for CD4, CD68, and CD45 were calculated. Clinical and histological features were compared between those with and without remission at week 22, and the factors associated with clinical outcomes were identified. We enrolled 42 patients. Patients with a high CD4+ infiltration showed a better response to vedolizumab [odds ratio (OR) = 1.44, P = 0.014]. The concomitant use of corticosteroids and high Mayo scores had a negative association with the vedolizumab response (OR = 0.11, P = 0.008 and OR = 0.50, P = 0.009, respectively). Histological evaluation for CD4+ cell infiltration may be helpful in selecting patients who can benefit from vedolizumab.
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