A monoclonal antibody against neem leaf glycoprotein recognizes carcinoembryonic antigen (CEA) and restricts CEA expressing tumor growth
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Updated: Apr 24, 2026

Enhancing Chimeric Antigen Receptor-Extracellular Vesicles (CAR-EV) Technology: The Future of Cancer Therapy
Published on: September 19, 2025
Arnab Das1, Subhasis Barik, Saptak Banerjee
1*Clinical Biochemistry Unit Departments of †Immunoregulation and Immunodiagnostics ∥Surgical Oncology and Medical Oncology, Chittaranjan National Cancer Institute ‡Department of Molecular Medicine, Bose Institute, Kolkata, India §Pediatric Hematology Oncology, University of Iowa Children's Hospital, IA.
Abstract:
Carcinoembryonic antigen (CEA) is one of the promising tumor antigens mainly associated with carcinoma of the colon, lung, breast, etc. and received wide attention for cancer immunotherapy. Neem leaf glycoprotein (NLGP), an effective immunomodulator, is able to generate humoral and cellular immune responses in murine tumor models. We have generated a monoclonal antibody (mAb) against NLGP by fusing NLGP-immunized mice splenocytes with nonsecretory myeloma cells. A highly anti-NLGP mAb secreting clone (1C8; IgG2a in nature) has been identified and propagated in culture. 1C8 recognizes human CEA as good as NLGP by enzyme linked immunosorbent assay, Western blotting, and immunoprecipitation. 1C8 detects CEA on colon cancer tissues by immunochistochemistry. By flow cytometry, 1C8 specifically reacts with CEA(+) human (Colo-205, HCT-116, and HT-29) and mouse (CT-26) colon cancer cells, but it showed minimum reactivity with CEA(-) human (MCF7, SiHa, and SCC084) and mouse (B16MelF10) cancer cells. This anti-NLGP 1C8 mAb revealed significant antitumor activity and better survivability in vivo in animals bearing mouse (CT-26 in BALB/c) and human (Colo-205 in athymic nude) CEA(+) cancer cells. 1C8 has no direct influence on proliferation and migration of CEA(+) cells, however, NK cell-dependent strong antibody-dependent cellular cytotoxicity reaction toward CEA(+) cells and normalization of angiogenesis are chiefly associated with tumor growth restriction. Obtained results provided a new immunotherapeutic approach for the effective management of CEA(+) tumors.
Insights
A new monoclonal antibody (mAb) targeting carcinoembryonic antigen (CEA) demonstrates significant antitumor activity against CEA-positive cancers. This antibody enhances survival by engaging natural killer cells and normalizing tumor angiogenesis, offering a novel cancer immunotherapy approach.
Area of Science:
- Immunology
- Oncology
- Biotechnology
Background:
- Carcinoembryonic antigen (CEA) is a key target in cancer immunotherapy, particularly for carcinomas.
- Neem leaf glycoprotein (NLGP) acts as an effective immunomodulator, stimulating immune responses in preclinical models.
Purpose of the Study:
- To develop a monoclonal antibody (mAb) against NLGP that also recognizes human CEA.
- To evaluate the therapeutic potential of this anti-CEA mAb in preclinical cancer models.
Main Methods:
- Generation of a monoclonal antibody (1C8, IgG2a) against NLGP.
- Characterization of 1C8's binding specificity to CEA using ELISA, Western blotting, immunoprecipitation, and flow cytometry.
- Assessment of 1C8's antitumor activity and efficacy in vivo in mouse and human cancer xenograft models.
Main Results:
- The 1C8 mAb specifically recognizes both NLGP and human CEA.
- 1C8 demonstrated significant antitumor activity and improved survival in CEA-positive colon cancer models.
- Tumor growth restriction was mediated by antibody-dependent cellular cytotoxicity (ADCC) and normalization of angiogenesis, not direct effects on cancer cell proliferation or migration.
Conclusions:
- The anti-NLGP 1C8 mAb is a promising therapeutic candidate for CEA-positive tumors.
- This antibody represents a novel immunotherapeutic strategy for managing various cancers expressing CEA.
- The mechanism involves immune cell activation and vascular normalization, highlighting a multifaceted approach to cancer treatment.
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