WT1 epitope-specific IgG and IgM antibodies for immune-monitoring in patients with advanced sarcoma treated with a WT1 peptide cancer vaccine.

WT1 antibody WT1 peptide cancer vaccine immune monitoring immunotherapy sarcoma

Journal

Oncology letters
ISSN: 1792-1082
Titre abrégé: Oncol Lett
Pays: Greece
ID NLM: 101531236

Informations de publication

Date de publication:
Feb 2022
Historique:
received: 09 10 2021
accepted: 03 12 2021
entrez: 24 1 2022
pubmed: 25 1 2022
medline: 25 1 2022
Statut: ppublish

Résumé

The Wilms' tumor gene WT1 is highly expressed in various malignancies and may be a common target antigen for cancer immunotherapy. In our group, peptide-based cancer vaccines targeting WT1 CTL epitopes were developed as an immunotherapy for these malignancies. In the present study, WT1 epitope-specific immune responses were analyzed in 31 patients with advanced sarcoma with human leukocyte antigen-A*24:02- and WT1-expressing tumors who received the WT1-235 peptide vaccine as monotherapy. The serum levels of IgG and IgM antibodies against the target epitope WT1-235 and the non-target epitopes WT1-332 and WT1-271 were measured using ELISA. IgM antibodies against WT1-235, WT1-332 and WT1-271 were detected in three (9.6%), four (12.9%) and 20 patients (64.5%), respectively, prior to vaccine administration, indicating immune recognition of the WT1 antigen prior to administering the vaccine. Of 15 patients who had completed the 3-month treatment protocol, WT1-235 IgG was positive in five (33.3%) patients. An enzyme-linked immunospot assay revealed that WT1-235 epitope-specific IL-10 production/secretion in peripheral blood mononuclear cells declined in the first month of vaccine administration in all three patients with positivity for WT1-235 IgM at the start of the vaccine. Furthermore, positivity for both WT1-235 and WT1-271 IgM antibodies at the start of treatment was associated with unfavorable tumor control at 3 months after vaccine administration. These results suggested that WT1 epitope-specific IgG and IgM antibodies may be utilized as immune-monitoring markers for WT1 peptide cancer vaccine immunotherapy. The trials were entered in the University hospital Medical Information Network (UMIN) Clinical Trials Registry (https://www.umin.ac.jp/ctr; no. UMIN000002001 on May 24, 2009 and no. UMIN000015997 on December 20, 2014).

Identifiants

pubmed: 35069874
doi: 10.3892/ol.2022.13184
pii: OL-23-02-13184
pmc: PMC8756391
doi:

Types de publication

Journal Article

Langues

eng

Pagination

65

Informations de copyright

Copyright: © Alzaaqi et al.

Déclaration de conflit d'intérêts

The authors declare that they have no competing interests.

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Auteurs

Shouq Alzaaqi (S)

Department of Clinical Laboratory and Biomedical Sciences, Osaka University Graduate School of Medicine, Suita, Osaka 565-0871, Japan.

Norifumi Naka (N)

Department of Orthopaedic Surgery, Nachikatsuura Town Onsen Hospital, Nachikatsuura, Wakayama 649-5331, Japan.

Kenichiro Hamada (K)

Hamada Orthopaedic Surgery, Kawanishi City, Hyogo 666-0021, Japan.

Naoki Hosen (N)

Department of Hematology and Oncology, Osaka University Graduate School of Medicine, Suita, Osaka 565-0871, Japan.

Mizuki Kanegae (M)

Department of Clinical Laboratory and Biomedical Sciences, Osaka University Graduate School of Medicine, Suita, Osaka 565-0871, Japan.

Hidetatsu Outani (H)

Department of Orthopaedic Surgery, Osaka University Graduate School of Medicine, Suita, Osaka 565-0871, Japan.

Mayuko Adachi (M)

Department of Clinical Laboratory and Biomedical Sciences, Osaka University Graduate School of Medicine, Suita, Osaka 565-0871, Japan.

Rin Imanishi (R)

Department of Clinical Laboratory and Biomedical Sciences, Osaka University Graduate School of Medicine, Suita, Osaka 565-0871, Japan.

Eiichi Morii (E)

Department of Pathology, Osaka University Graduate School of Medicine, Suita, Osaka 565-0871, Japan.

Miki Iwai (M)

Department of Clinical Laboratory and Biomedical Sciences, Osaka University Graduate School of Medicine, Suita, Osaka 565-0871, Japan.

Jun Nakata (J)

Department of Clinical Laboratory and Biomedical Sciences, Osaka University Graduate School of Medicine, Suita, Osaka 565-0871, Japan.

Fumihiro Fujiki (F)

Department of Cancer Immunology, Osaka University Graduate School of Medicine, Suita, Osaka 565-0871, Japan.

Soyoko Morimoto (S)

Department of Cancer Stem Cell Biology, Osaka University Graduate School of Medicine, Suita, Osaka 565-0871, Japan.

Hiroko Nakajima (H)

Department of Cancer Immunology, Osaka University Graduate School of Medicine, Suita, Osaka 565-0871, Japan.

Sumiyuki Nishida (S)

Department of Respiratory Medicine and Clinical Immunology, Osaka University Graduate School of Medicine, Suita, Osaka 565-0871, Japan.

Akihiro Tsuboi (A)

Department of Cancer Immunotherapy, Osaka University Graduate School of Medicine, Suita, Osaka 565-0871, Japan.

Yoshihiro Oka (Y)

Department of Cancer Stem Cell Biology, Osaka University Graduate School of Medicine, Suita, Osaka 565-0871, Japan.
Department of Respiratory Medicine and Clinical Immunology, Osaka University Graduate School of Medicine, Suita, Osaka 565-0871, Japan.
Department of Immunopathology, World Premier International Research Center, Immunology Frontier Research Center, Osaka University, Suita, Osaka 565-0871, Japan.

Haruo Sugiyama (H)

Department of Cancer Immunology, Osaka University Graduate School of Medicine, Suita, Osaka 565-0871, Japan.

Yusuke Oji (Y)

Department of Clinical Laboratory and Biomedical Sciences, Osaka University Graduate School of Medicine, Suita, Osaka 565-0871, Japan.

Classifications MeSH