2021
DOI: 10.1080/08830185.2021.1960986
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Antibody engineering and its therapeutic applications

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Cited by 10 publications
(4 citation statements)
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“…Previously, the generation of antibody fragments, specifically Fab and (Fab)2 0 , relied on proteolytic cleavage of classical antibodies. 46,48,49 However, Plückthun and Skerra have outlined an alternative approach using cloning vectors to produce fully functional Fv and Fab fragments. By employing cloning vectors, antibodies can be directed into the periplasmic space, benefitting from the oxidizing environment that facilitates disulfide bond formation.…”
Section: Discussionmentioning
confidence: 99%
See 1 more Smart Citation
“…Previously, the generation of antibody fragments, specifically Fab and (Fab)2 0 , relied on proteolytic cleavage of classical antibodies. 46,48,49 However, Plückthun and Skerra have outlined an alternative approach using cloning vectors to produce fully functional Fv and Fab fragments. By employing cloning vectors, antibodies can be directed into the periplasmic space, benefitting from the oxidizing environment that facilitates disulfide bond formation.…”
Section: Discussionmentioning
confidence: 99%
“…Bioengineered antibodies exhibit characteristics such as low molecular mass, high physicochemical stability, increased flexibility, and easy accessibility to antigens, making them potential substitutes that emulate naturally generated antibodies. Previously, the generation of antibody fragments, specifically Fab and (Fab)2′, relied on proteolytic cleavage of classical antibodies 46,48,49 . However, Plückthun and Skerra have outlined an alternative approach using cloning vectors to produce fully functional Fv and Fab fragments.…”
Section: Discussionmentioning
confidence: 99%
“…Targeted therapy and diagnostic imaging can be carried out on a flexible platform so that these proteins can be arranged to bind preferentially to cancerassociated indicators. Relative to conventional antibodies, engineered proteins provide the benefit of lower immunogenicity [10]. However, since they can be expensive and hard to produce, additional optimization is required to make the manufacturing process more efficient.…”
Section: Multistep Glycosylation Proteins Targeting Agentsmentioning
confidence: 99%
“…Production of humanized and fully human antibodies has been evolved tremendously for medical purposes to reduce the immunogenicity of the non-human isotype [ 27 ]. Moreover, the intact four chain-mAb molecule has demonstrated clinical disadvantages, such as poor tissue penetration and slow blood clearance due to the large size (~150 kDa), and particularly induced proinflammatory responses due to the presence of the Fc portion, which can interact and activate effector cells and the complement cascade [ 27 , 28 ]. Thus, Ab engineering has been investigated to reduce the immunogenicity of Ab for medical use.…”
Section: Introductionmentioning
confidence: 99%