TY - JOUR
T1 - Selective targeting of multiple myeloma cells with a monoclonal antibody recognizing the ubiquitous protein CD98 heavy chain
AU - Hasegawa, Kana
AU - Ikeda, Shunya
AU - Yaga, Moto
AU - Watanabe, Kouki
AU - Urakawa, Rika
AU - Iehara, Akie
AU - Iwai, Mai
AU - Hashiguchi, Seishin
AU - Morimoto, Soyoko
AU - Fujiki, Fumihiro
AU - Nakajima, Hiroko
AU - Nakata, Jun
AU - Nishida, Sumiyuki
AU - Tsuboi, Akihiro
AU - Oka, Yoshihiro
AU - Yoshihara, Satoshi
AU - Manabe, Masahiro
AU - Ichihara, Hiroyoshi
AU - Mugitani, Atsuko
AU - Aoyama, Yasutaka
AU - Nakao, Takafumi
AU - Hirose, Asao
AU - Hino, Masayuki
AU - Ueda, Shiho
AU - Takenaka, Katsuto
AU - Masuko, Takashi
AU - Akashi, Koichi
AU - Maruno, Takahiro
AU - Uchiyama, Susumu
AU - Takamatsu, Shinji
AU - Wada, Naoki
AU - Morii, Eiichi
AU - Nagamori, Shushi
AU - Motooka, Daisuke
AU - Kanai, Yoshikatsu
AU - Oji, Yusuke
AU - Nakagawa, Tomoyoshi
AU - Kijima, Noriyuki
AU - Kishima, Haruhiko
AU - Ikeda, Atsuyo
AU - Ogino, Takayuki
AU - Shintani, Yasushi
AU - Kubo, Tateki
AU - Mihara, Emiko
AU - Yusa, Kosuke
AU - Sugiyama, Haruo
AU - Takagi, Junichi
AU - Miyoshi, Eiji
AU - Kumanogoh, Atsushi
AU - Hosen, Naoki
N1 - Funding Information:
We thank T. Yamane (Osaka City General Hospital), K. Koh (Osaka General Hospital for West Japan Railway Company), and M. Ichii (Osaka University Graduate School of Medicine) for MM samples; T. Kitamura (The University of Tokyo) for the retroviral vectors; and Y. Kanakura (Osaka University), R. Burger (University of Kiel), and I. Weissman (Stanford University) for the cell lines. We also thank K. Terasaki, Y. Hayami, R. Inada, M. Yamaguchi, T. Wibowo, T. Uehara, and M. Matsubara for technical assistance. Editorial services were provided by N. R. Gough (BioSerendipity LLC, Elkridge, MD). This work was supported in part by the Japan Agency for Medical Research and Development (AMED) (20cm0106361h0002 to N.H. and JP18cm016335 and JP18cm059042 to A.K.), the Center of Innovation Program (COI STREAM) from the Ministry of Education, Culture, Sports, Science and Technology of Japan (MEXT) (to A.K.), the Japan Society for the Promotion of Science (JSPS) KAKENHI (JP19K16799 and JP21K15487 to K.H., JP26461404 and JP20H03710 to N.H., and JP18H05282 to A.K.), grants from the Kansai Economic Federation (KANKEIREN) (to A.K.), the Mitsubishi Foundation (to A.K.), the Yasuda Kinen Medical Foundation (to N.H.), the SENSHIN Medical Research Foundation (to N.H.), KAKETSUKEN (to N.H.), the Uehara Memorial Foundation (to N.H.), the Astellas Foundation for Research on Metabolic Disorders (to N.H.), and the Takeda Science Foundation (to N.H.).
Publisher Copyright:
© 2022 The Authors, some rights reserved
PY - 2022/2/16
Y1 - 2022/2/16
N2 - Cancer-specific cell surface antigens are ideal therapeutic targets for monoclonal antibody (mAb)-based therapy. Here, we report that multiple myeloma (MM), an incurable hematological malignancy, can be specifically targeted by an mAb that recognizes a ubiquitously present protein, CD98 heavy chain (hc) (also known as SLC3A2). We screened more than 10,000 mAb clones raised against MM cells and identified R8H283, an mAb that bound MM cells but not normal hematopoietic or nonhematopoietic cells. R8H283 specifically recognized CD98hc. R8H283 did not react with monomers of CD98hc; instead, it bound CD98hc in heterodimers with a CD98 light chain (CD98lc), a complex that functions as an amino acid transporter. CD98 heterodimers were abundant on MM cells and took up amino acids for constitutive production of immunoglobulin. Although CD98 heterodimers were also present on normal leukocytes, R8H283 did not react with them. The glycoforms of CD98hc present on normal leukocytes were distinct from those present on MM cells, which may explain the lack of R8H283 reactivity to normal leukocytes. R8H283 exerted anti-MM effects without damaging normal hematopoietic cells. These findings suggested that R8H283 is a candidate for mAb-based therapies for MM. In addition, our findings showed that a cancer-specific conformational epitope in a ubiquitous protein, which cannot be identified by transcriptome or proteome analyses, can be found by extensive screening of primary human tumor samples.
AB - Cancer-specific cell surface antigens are ideal therapeutic targets for monoclonal antibody (mAb)-based therapy. Here, we report that multiple myeloma (MM), an incurable hematological malignancy, can be specifically targeted by an mAb that recognizes a ubiquitously present protein, CD98 heavy chain (hc) (also known as SLC3A2). We screened more than 10,000 mAb clones raised against MM cells and identified R8H283, an mAb that bound MM cells but not normal hematopoietic or nonhematopoietic cells. R8H283 specifically recognized CD98hc. R8H283 did not react with monomers of CD98hc; instead, it bound CD98hc in heterodimers with a CD98 light chain (CD98lc), a complex that functions as an amino acid transporter. CD98 heterodimers were abundant on MM cells and took up amino acids for constitutive production of immunoglobulin. Although CD98 heterodimers were also present on normal leukocytes, R8H283 did not react with them. The glycoforms of CD98hc present on normal leukocytes were distinct from those present on MM cells, which may explain the lack of R8H283 reactivity to normal leukocytes. R8H283 exerted anti-MM effects without damaging normal hematopoietic cells. These findings suggested that R8H283 is a candidate for mAb-based therapies for MM. In addition, our findings showed that a cancer-specific conformational epitope in a ubiquitous protein, which cannot be identified by transcriptome or proteome analyses, can be found by extensive screening of primary human tumor samples.
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U2 - 10.1126/scitranslmed.aax7706
DO - 10.1126/scitranslmed.aax7706
M3 - Article
C2 - 35171652
AN - SCOPUS:85124778405
VL - 14
JO - Science Translational Medicine
JF - Science Translational Medicine
SN - 1946-6234
IS - 632
M1 - eaax7706
ER -