"Personalised mRNA cancer vaccine shows 49% reduction in melanoma death risk"
Neoantigen
tumour-specific protein produced by cancer mutations, absent from healthy cells, unique to each patient.
mRNA vaccine
delivers genetic instructions for cells to produce a target protein, training immune response without live pathogen.
Vaccines have traditionally worked by introducing a pathogen's antigen, a protein or inactivated fragment, to train the immune system to recognise and fight future infections. The development of mRNA vaccine technology, accelerated by the COVID-19 pandemic, changed this paradigm. Instead of delivering a protein directly, mRNA vaccines deliver genetic instructions that tell the body's own cells to produce the target protein. This approach is faster to design, scalable, and does not require live pathogens. Recombinant DNA technology and advances in lipid nanoparticle delivery systems made mRNA vaccines clinically viable.
Cancer immunotherapy represents a parallel revolution. The immune system can, in principle, recognise and destroy cancer cells, but tumours evolve mechanisms to evade detection. Checkpoint inhibitor drugs like pembrolizumab (sold as Keytruda) work by blocking proteins that cancer cells use to suppress immune responses. Keytruda has shown strong efficacy across several cancers, including melanoma, lung cancer, and certain head-and-neck cancers. The convergence of mRNA technology and cancer immunotherapy has opened the door to personalised therapeutic vaccines, vaccines designed not to prevent infection, but to treat an existing disease by re-arming the immune system.
India's cancer burden is significant. The country faces a dual challenge: a rising incidence of cancers driven by lifestyle, environmental, and genetic factors, alongside severe constraints in treatment access. Immunotherapy drugs are among the most expensive cancer treatments globally, and India's public health infrastructure, built around the Universal Immunisation Programme (UIP) and the National Health Mission (NHM), is primarily oriented toward preventive vaccines for infectious diseases, not therapeutic oncology.
The personalised cancer vaccine intismeran works by identifying the unique mutational fingerprint of an individual patient's tumour. Tumour cells carry abnormal proteins called neoantigens, proteins produced by cancer-specific mutations that are absent from healthy cells. Because neoantigens differ from patient to patient, the vaccine must be custom-designed for each individual. Scientists sequence the patient's tumour sample, identify the most immunologically relevant mutations, and synthesise mRNA strands encoding up to 34 neoantigens. Once injected, the body's cells read these mRNA instructions, produce the neoantigen proteins, and present them to the immune system. The immune system then learns to recognise these proteins as foreign and mounts a targeted response against any cell displaying them.
This mechanism is conceptually identical to a conventional vaccine, teach the immune system to recognise a specific target, but the target is the patient's own cancer rather than a pathogen. …
Which one of the following statements best describes the role of B cells and T cells in the human body?
In the context of vaccines manufactured to prevent COVID-19 pandemic, consider the following statements:
1.The Serum Institute of India produced COVID-19 vaccine named Covishield using mRNA platform.
2.Sputnik V vaccine is manufactured using vector based platform.
3.COVAXIN is an inactivated pathogen based vaccine.
Which of the statements given above are correct?
Which one of the following statements is not correct?
Which one of the following best describes the function of neoantigens in the context of personalised cancer vaccines?
Consider the following statements about mRNA vaccine technology:
1.mRNA vaccines deliver genetic instructions that cause the body's cells to produce a target protein, which then trains the immune system.
2.mRNA vaccines carry a risk of pathogen reactivation because they contain live attenuated virus.
3.The mRNA platform can be rapidly redesigned for new targets, including cancer-specific neoantigens.
Which of the statements given above are correct?
Want the full note, Prelims Facts & MCQ answers?
Create a free account — takes less than a minute.
Create free account