Abstract

Protein based therapeutics have been regarded very highly as they have produced immense results in treating various diseases including genetic disorders, neurodegenerative disorders, sexually transmitted diseases, and autoimmune disorders. This has revolutionized the field of medicine by enabling precise targeting for treating diseases and personalized medicine for different individuals. The ability to target the source of a disease or disorder has made this line of therapeutics a major outbreak for revolutionizing the field of targeted medicine and is currently being pursued for developing novel therapeutics. The production of recombinant protein paved the way for these therapeutics and despite the considerable progress made so far in the study and production of therapeutic proteins, there are still concerns over its off-target effects and ethical considerations, which have spurred the exploration of alternative approaches. In this context, this article is presented on therapeutic proteins, an innovative biological approach that has the potential to cure disorders that were once considered incurable. This article highlights the limitations of current targeted medicine technologies and the need for more targeted and personalized approaches to treat genetic disorders. Employing artificially synthesized therapeutic proteins such as monoclonal antibodies (MAC) to target specific cells, tissues, organs, genes, proteins, and sites of disease progression has proven to be more effective in treating the diseases. This approach provides greater specificity and control over various disorders, making it a highly promising therapeutic option for various diseases such as cancer, cardiovascular diseases, and viral infections. This article discusses the status of therapeutic proteins, their potential prospects, as well as the challenges and opportunities that need to be addressed to fully exploit their potential. Overall, the article aims to shed light on the significance of therapeutic medicine in the field of medicine and its potential to revolutionize treatments for various disorders. By providing an overview of this innovative approach, it hopes to inspire further research in this area and pave the way for novel and more effective therapies for genetic disorders.

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