“…2 d, f), which can be selected from synthetic, naive, or immunized cDNA libraries using phage, bacterial, yeast, or ribosomal display technologies [ 233 – 235 ]. Nbs have the smallest structures (~ 13 kDa) compared with other Abs, present with antigenic recognition, can act in a monomeric form or fusion protein, and show high specificity, stability, and solubility [ 236 ]. Therefore, Nbs are valuable in biomedical research.…”
Section: Insights From Ab Therapeutic Strategies Against Sars-cov-2 Infectionmentioning
SARS-CoV-2 is a novel β-coronavirus that caused the COVID-19 pandemic disease, which spread rapidly, infecting more than 134 million people, and killing almost 2.9 million thus far. Based on the urgent need for therapeutic and prophylactic strategies, the identification and characterization of antibodies has been accelerated, since they have been fundamental in treating other viral diseases. Here, we summarized in an integrative manner the present understanding of the immune response and physiopathology caused by SARS-CoV-2, including the activation of the humoral immune response in SARS-CoV-2 infection and therefore, the synthesis of antibodies. Furthermore, we also discussed about the antibodies that can be generated in COVID-19 convalescent sera and their associated clinical studies, including a detailed characterization of a variety of human antibodies and identification of antibodies from other sources, which have powerful neutralizing capacities. Accordingly, the development of effective treatments to mitigate COVID-19 is expected. Finally, we reviewed the challenges faced in producing potential therapeutic antibodies and nanobodies by cell factories at an industrial level while ensuring their quality, efficacy, and safety.
“…2 d, f), which can be selected from synthetic, naive, or immunized cDNA libraries using phage, bacterial, yeast, or ribosomal display technologies [ 233 – 235 ]. Nbs have the smallest structures (~ 13 kDa) compared with other Abs, present with antigenic recognition, can act in a monomeric form or fusion protein, and show high specificity, stability, and solubility [ 236 ]. Therefore, Nbs are valuable in biomedical research.…”
Section: Insights From Ab Therapeutic Strategies Against Sars-cov-2 Infectionmentioning
SARS-CoV-2 is a novel β-coronavirus that caused the COVID-19 pandemic disease, which spread rapidly, infecting more than 134 million people, and killing almost 2.9 million thus far. Based on the urgent need for therapeutic and prophylactic strategies, the identification and characterization of antibodies has been accelerated, since they have been fundamental in treating other viral diseases. Here, we summarized in an integrative manner the present understanding of the immune response and physiopathology caused by SARS-CoV-2, including the activation of the humoral immune response in SARS-CoV-2 infection and therefore, the synthesis of antibodies. Furthermore, we also discussed about the antibodies that can be generated in COVID-19 convalescent sera and their associated clinical studies, including a detailed characterization of a variety of human antibodies and identification of antibodies from other sources, which have powerful neutralizing capacities. Accordingly, the development of effective treatments to mitigate COVID-19 is expected. Finally, we reviewed the challenges faced in producing potential therapeutic antibodies and nanobodies by cell factories at an industrial level while ensuring their quality, efficacy, and safety.
“…Permeabilization can be increased through a combination of detergents, collagenases, acids, denaturants, temperature changes and long, up to weeks, antibody incubation times (Hahn et al, 2021;Hong et al, 2019;Molbay et al, 2021;Noë et al, 2018). As the size of antibodies determines their ability to penetrate tissues, nanobodies, which are small (~15kDa versus monoclonal antibodies which are ~150kDa) single domain antibodies found in Camelidae (Alpaca, Llama), are emerging as a versatile option (Chames and Rothbauer, 2020;Jailkhani et al, 2019;Ramos-Gomes et al, 2018;Rousserie et al, 2015). The next step is to overcome the opaqueness of tissues.…”
“…In addition, nanobodies can tolerate more challenging conditions, such as higher temperatures. Merging the advantages of small molecules and antibodies, nanobodies have become an emerging scaffold for PET tracers after its main patent expired in the late 2010s [ 88 ]. Other potential vectors include affibodies, DARPins, and affimers [ 89 , 90 , 91 ].…”
Non-invasive positron emission tomography (PET) imaging of immune cells is a powerful approach for monitoring the dynamics of immune cells in response to immunotherapy. Despite the clinical success of many immunotherapeutic agents, their clinical efficacy is limited to a subgroup of patients. Conventional imaging, as well as analysis of tissue biopsies and blood samples do not reflect the complex interaction between tumour and immune cells. Consequently, PET probes are being developed to capture the dynamics of such interactions, which may improve patient stratification and treatment evaluation. The clinical efficacy of cancer immunotherapy relies on both the infiltration and function of cytotoxic immune cells at the tumour site. Thus, various immune biomarkers have been investigated as potential targets for PET imaging of immune response. Herein, we provide an overview of the most recent developments in PET imaging of immune response, including the radiosynthesis approaches employed in their development.
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