Cloning and molecular characterization of the cDNAs encoding the variable regions of an anti-CD20 monoclonal antibody.
Cloning and molecular characterization of the cDNAs encoding the variable regions of an anti-CD20 monoclonal antibody.
نویسندگان: داریوش شانه بندی , جعفر مجیدی ذوالبین , توحید کاظمی , بهزاد برادران , لیلی عاقبتی
کلمات کلیدی: CD20, targeted therapy, monoclonal antibody, bispecific antibody, chimeric antigen receptor, antibody drug conjugate
نشریه: 14092 , 1 , 26 , 2017
| نویسنده ثبت کننده مقاله |
جعفر مجیدی ذوالبین |
| مرحله جاری مقاله |
تایید نهایی |
| دانشکده/مرکز مربوطه |
مرکز تحقیقات ایمونولوژی |
| کد مقاله |
61097 |
| عنوان فارسی مقاله |
Cloning and molecular characterization of the cDNAs encoding the variable regions of an anti-CD20 monoclonal antibody. |
| عنوان لاتین مقاله |
Cloning and molecular characterization of the cDNAs encoding the variable regions of an anti-CD20 monoclonal antibody. |
| ناشر |
5 |
| آیا مقاله از طرح تحقیقاتی و یا منتورشیپ استخراج شده است؟ |
بلی |
| عنوان نشریه (خارج از لیست فوق) |
|
| نوع مقاله |
Original Article |
| نحوه ایندکس شدن مقاله |
ایندکس شده سطح دو – Medline |
| آدرس لینک مقاله/ همایش در شبکه اینترنت |
http://content.iospress.com/articles/human-antibodies/hab314 |
| Abstract.
BACKGROUND: CD20-based targeting of B-cells in hematologic malignancies and autoimmune disorders is associated with
outstanding clinical outcomes. Isolation and characterization of VH and VL cDNAs encoding the variable regions of the heavy
and light chains of monoclonal antibodies (MAb) is necessary to produce next generation MAbs and their derivatives such as and
bispecific antibodies (bsAb) and single-chain variable fragments (scFv).
OBJECTIVE: This study was aimed at cloning and characterization of the VH and VL cDNAs from a hybridoma cell against
the CD20 antigen.
METHODS: VH and VL fragments were amplified, cloned and characterized. Furthermore, amino acid sequences of VH, VL
and corresponding complementarity-determining regions (CDR) were compared with those of four approved MAbs including
Rituximab (RTX), Ibritumomab tiuxetan, Ofatumumab and GA101.
RESULTS: The cloned VH and VL cDNAs were found to be functional and follow a consensus pattern. A noticeable similarity
between the VH and VL amino acid sequences with those of RTX and Ibritumomab was evident. Furthermore, amino acid
sequences of VH and VL CDRs indicated significant similarities to RTX and Ibritumomab CDRs.
CONCLUSIONS: Successful recovery of VH and VL fragments encourages the development of novel CD20 targeting bsAbs,
scFvs, antibody conjugates and T-cells armed with chimeric antigen receptors. |
| نام فایل |
تاریخ درج فایل |
اندازه فایل |
دانلود |
| shanehbandi2017.pdf | 1396/05/09 | 1296460 | دانلود |