Antibody humanization is a crucial biotechnological process designed to transform non-human antibodies into human-like structures. This process significantly reduces immunogenicity while retaining the original antibody's specificity and affinity for its target antigen. Creative Biolabs, a leader in the field of antibody engineering, offers cutting-edge antibody humanization services tailored to diverse research needs.
Through the flourish of antibody based therapeutic drugs, the demand of human or humanized antibody is synchronized growth. Due to the potential risk of immunogenicity, the full human antibody or at least humanized antibody (from xenogeneic sources) is required for further clinical application. Because of the serious ethical and moral issues, it is obviously an impossible task to directly immunize human beings with interested antigens. Nevertheless, Creative Biolabs is able to provide human or humanized antibodies in the ethical standards category by three techniques to overcome this limitation.
Creative Biolabs owns several naive or synthetic human antibody libraries in-house with diversity of over 109. These premade antibody libraries are generally based on human antibody genes from non-immunized donors or human antibody repertoire and constructed in scFv or Fab format. In this way, these premade libraries are qualified for screening human antibodies specific binding to the target protein (or other molecules). Owe to the 100% human sources, the isolated antibodies carry rare risk to cause significant immunogenicity issue in therapeutic applications.
Another choice for producing fully human antibody is utilizing the Fully Human Antibody Technology™ (FHAT) of Creative Biolabs. This technology is based on the creation of a mouse strain engineered to produce a large repertoire of human antibodies in the absence of mouse antibodies. Through introducing human immunoglobulin loci into the germline of mice deficient in mouse antibody production, the "humanized" transgenic mice (FHAT transgenic mice) are able to produce significant levels of antigen-specific human antibodies with high affinity and specificity.
Creative Biolabs has developed the innovative Hi-AffiTM platform to provide top-class humanization of non-human primate (NHP) antibody as a unique solution to develop therapeutic antibodies for human use. Compared with the commonly used rodent, NHP has much closer genetic relationship to that of human, which means that the antibodies isolated from immunized NHPs may have higher affinity and lower immunogenicity to human beings. On the other hand, the humanization of NHP antibody is much easier than other species, and potentially has no affinity loss under suitable technique.
Besides non-human primate, Creative Biolabs also provide humanization service to antibodies derived from other species, such as mouse, rat, rabbit, chicken, llama, dog, shark and more.
Creative Biolabs offers comprehensive human or humanized antibody services, combining over 20 years of expertise with advanced technologies to ensure minimal immunogenicity and high antigen-binding affinity. Alongside traditional CDR grafting, we provide access to human antibodies from premade human antibody libraries for rapid discovery, fully human antibodies from FHAT transgenic mice for natural immune-derived solutions, and specialized NHP antibody humanization to retain unique binding properties. These tailored services support therapeutic target validation, diagnostic assay development, and preclinical research with unparalleled precision and quality.
Fig. 3 Neutralizing activity of EV2038 in vitro.1
Human cytomegalovirus can cause serious diseases in children and immunocompromised patients. Here, the researchers studied the inhibitory effects of whole-human neutralizing monoclonal antibodies on human cytomegalovirus infection and virus-to-cell transmission. The scientists isolated a potent neutralizing antibody EV2038 (IgG1 lambda) that inhibits human cytomegalovirus infection in all four laboratory strains and 42 clinical isolates. In addition, EV2038 can prevent the intercellular transmission of eight clinical virus isolates. EV2038 can recognize three discontinuous sequences on glycoprotein B antigen domain 1, which are highly conserved in many clinical isolates. The data in this article show that EV2038 is expected to be a candidate and a new alternative drug for the treatment of human cytomegalovirus infection.
Human antibodies are produced naturally by the immune system in humans. They are derived from B cells and are fully human in their protein structure, which minimizes the risk of immune reactions when used in therapeutic applications. Humanized antibodies, on the other hand, are originally derived from non-human species, typically mice. These antibodies are then genetically engineered by replacing most of the mouse protein sequences with human sequences while retaining the small regions critical for antigen binding. This process reduces the immunogenicity of the antibodies when used in human therapy, making them more suitable for repeated administration in chronic conditions.
Humanized antibodies play a crucial role in the treatment of chronic diseases such as cancer, autoimmune diseases, and various infectious diseases. Their importance lies in their ability to specifically target diseased cells or pathological molecules with minimal side effects compared to traditional drugs. By modifying mouse antibodies to resemble human antibodies more closely, humanized antibodies can be administered to patients without significant risk of immune rejection. This makes them effective tools in targeted therapies, where precision and reduced side effects are paramount.
Human and humanized antibodies are pivotal in the field of immunotherapy, particularly in the treatment of diseases where the immune system plays a key role, such as cancer, autoimmune disorders, and infections. These antibodies can be designed to perform a variety of functions, such as blocking the activity of a specific protein, marking cancer cells for destruction by the immune system, or modulating immune responses. For example, in cancer treatment, antibodies can be engineered to target and bind to cancer cell-specific antigens, leading to direct cell killing or recruitment of other immune cells to eliminate the tumor. In autoimmune diseases, these antibodies can help dampen overactive immune responses, thereby reducing inflammation and tissue damage.
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