As our recent article outlines, cell & gene therapies (CGTs) offer life-sustaining medicinal products, but face challenges in adopting robust and well-characterized biomanufacturing processes. Raw materials play an important, early role in controlling the overall quality, safety, and efficacy of the final products. For CGTs, raw materials are reagents, solvents, substances, or components used in the manufacturing process, but are not intended to be part of the final therapeutic product. A common issue is variability in raw materials that, in turn, could lead to underperformance and batch failures.

 

Adopting raw materials for CGT manufacturing that comply with regulatory requirements, including GMP and other quality standards, goes a long way to ensure biomanufacturers can properly evaluate the suitability of materials for their own process. Overall, best practices recommended by regulatory experts is for biomanufacturers to use GMP-grade and animal-derived component-free (ADCF) raw materials, procured from safe and traceable sources to achieve the most control and consistency in their process. This reduces potential roadblocks to a scalable supply chain and smooths the transfer path between research, clinical, and manufacturing partners⁵.

 

Animal-derived components, such as fetal bovine serum (FBS), are heterogeneous in nature, which negatively impacts product consistency⁵. For T cell activation procedures, BioLegend manufactures monoclonal antibodies Cell-Vive™ GMP Ultra-LEAF™ Purified anti-human CD3 SF Antibody (clone OKT3) and GMP Ultra-LEAF™ Purified anti-human CD28 SF Antibody (clone S20013F) under serum-free (SF) conditions, from start to finish. We also offer biotinylated formats, such as GMP Ultra-LEAF™ Biotin anti-human CD3 SF Antibody and Cell-Vive™ GMP Ultra-LEAF™ Biotin anti-human CD28 SF Antibody, ideal as probes to facilitate T cell research or T cell separation .

 

Our CD3 and CD28 antibodies are optimized for T cell activation and expansion in ex vivo cell culture applications.

 

 

We source the highest quality raw materials to manufacture these SF antibodies, thus removing risk while providing additional control, consistency, and safety for T cell-based workflows.

 

BioLegend GMP Ultra-LEAF™ SF antibody specifications:

• Purification by affinity chromatography under azide-free conditions and filtration through a 0.1 µm membrane.
• QC testing to be bioburden negative.
• Ultra-low in endotoxin (<0.01 EU/µg of protein).
• Validation testing by flow cytometry.
• Ultra-LEAF™ formulation which comes with quality testing by functional assays.
• Manufactured in a dedicated GMP facility that is ISO 13485:2016 and MDSAP certified, monitored through independent QA oversight.
• Manufactured and tested in accordance with USP Chapter 1043, Ancillary Materials for Cell, Gene and Tissue-Engineered Products and Ph. Eur. Chapter 5.2.12.
• Complete raw material traceability and documentation support.
• DMF support will be available.

By following GMP, BioLegend manufactures these CD3 and CD28 antibodies under standardized conditions and processes governed by quality oversight. This ensures they are produced in a controlled manner. In addition, we source the highest quality raw materials to manufacture all of our GMP SF bioprocessing reagents, thus helping to reduce batch-to-batch variability and improving the overall consistency of the final product. As a partner to biomanufacturers, we understand the importance of being a reliable and trustworthy supplier of high-quality materials that are manufactured in GMP-certified facilities. This ultimately reduces the burden of qualification on CGT manufacturers, facilitating translation from research to later stage development and marketing⁶.

 

Our scientists recognize the current challenges for the cell therapy industry. In addition to GMP SF functional CD3 and CD28 antibodies, we offer novel SF and chemically-defined GMP cell culture reagents to achieve controlled cell culture environments for the expansion, activation, and differentiation of T cells. Biomanufacturers can make use of our non-GMP solutions that can be implemented across the T cell therapy workflow to seamlessly transition from R&D to clinical applications. We also provide custom GMP development and manufacturing services for antibodies and ancillary reagents based on customer-specific program requirements. As your trusted partner, we want to enable your research so it leads to greater insights to T cell development and function, leading to improved therapeutics. Explore our entire workflow solutions.

 

References

1. Xia, Fan et al. “TCR and CD28 Concomitant Stimulation Elicits a Distinctive Calcium Response in Naive T Cells.” Frontiers in immunology vol. 9 2864. 4 Dec. 2018, doi:10.3389/fimmu.2018.02864. PubMed.
2. Mukherjee, Anirban Goutam et al. “Role of Immune Cells and Receptors in Cancer Treatment: An Immunotherapeutic Approach.” Vaccines vol. 10,9 1493. 7 Sep. 2022, doi:10.3390/vaccines10091493. PubMed.
3. Reynolds, Sharon. “Engineering Car T-Cell Therapy to Overcome Limitations.” National Cancer Institute, NIH, 8 Feb. 2023, https://www.cancer.gov/news-events/cancer-currents-blog/2023/car-t-cell-therapies-overcoming-limitations.
4. Li, Hongwen et al. “Preclinical and clinical studies of CAR-NK-cell therapies for malignancies.” Frontiers in immunology vol. 13 992232. 24 Oct. 2022, doi:10.3389/fimmu.2022.992232. PubMed.
5. Bhattacharya, Sam, and Aparna Telang. “Manufacturing and Qualification Challenges for Cell and Gene Therapy Products and Best Practices for Success.” Cell Culture Dish, BioLegend, 6 Mar. 2023, https://cellculturedish.com/manufacturing-and-qualification-challenges-for-cell-and-gene-therapy-products-and-best-practices-for-success/.
6. Tsokas, Katherine et al. “Reducing Risks and Delays in the Translation of Cell and Gene Therapy Innovations into Regulated Products.” NAM perspectives vol. 2019 10.31478/201909d. 30 Sep. 2019, doi:10.31478/201909d. PubMed.