Developing and characterizing a single-domain antibody (nanobody) against human cytotoxic T-lymphocyte-associated protein ۴ (hCTLA-۴)

سال انتشار: 1400
نوع سند: مقاله ژورنالی
زبان: انگلیسی
مشاهده: 244

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شناسه ملی سند علمی:

JR_IJBMS-24-9_013

تاریخ نمایه سازی: 24 شهریور 1400

چکیده مقاله:

Objective(s): Cytotoxic T-lymphocyte-associated protein-۴ (CTLA-۴) is the most important human immune checkpoint that modulates T cells activity and brings about immune-homeostasis. Accordingly, checkpoint inhibitor cancer therapy has been approved as a growing method to block over-expressed immune checkpoints, such as CTLA-۴ receptors. Considering the competitive characteristics of single-domain antibodies with monoclonal antibodies, we tried to develop a camelid Nanobody against human CTLA-۴. Materials and Methods: We have constructed the VHH gene library by using immunized-camel peripheral blood mononuclear cells and carrying out the Nested-PCR technique. VHH-library was screened by phage display technique and specific nanobodies against CTLA-۴ protein were selected and amplified with bio-panning steps. Stronger binders were screened by Periplasmic Extract-ELISA, followed by estimating the complexity of the library. Specific anti-CTLA-۴ Nanobody and ۳hCTL۵۵, with longer CDR۳ and a higher binding rate, were selected for more assays. Results: Results revealed the existence of two different clones in the library with ۱۰۸ binders. In comparison with seven different antigens, using the ELISA technique confirmed the specificity of Nanobody ۳hCTL۵۵ against human CTLA-۴ antigen. We calculated Nanobody ۳hCTL۵۵ affinity for human CTLA-۴ antigen at ۵۰×۱۰-۹ M, approximately. Performing western blot and Flow-cytometry techniques showed that Nanobody ۳hCTL۵۵ was able to specifically detect and attach both commercial human CTLA-۴ protein and human CTLA-۴ antigen on the cell surface and in the cell lysate. Conclusion: Taken together, this developed camelid-specific anti-CTLA-۴ Nanobody ۳hCTL۵۵, selected from a high-quality immune library by phage display technique, may be effective for further study about cancer diagnosis and cancer-therapy purposes.

نویسندگان

Nazli Sotoudeh

Department of Biology, Science and Research Branch, Islamic Azad University, Tehran, Iran

Zahra Noormohammadi

Department of Biology, Science and Research Branch, Islamic Azad University, Tehran, Iran

Mahdi Habibi-Anbouhi

National Cell Bank of Iran, Pasteur Institute of Iran, Tehran, Iran

Fatemeh Kazemi-Lomedasht

Biotechnology Research Center, Venom and Biotherapeutics Molecules Laboratory, Pasteur Institute of Iran, Tehran, Iran

Mahdi Behdani

Biotechnology Research Center, Venom and Biotherapeutics Molecules Laboratory, Pasteur Institute of Iran, Tehran, Iran

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