Neoantigens in Chronic Obstructive Pulmonary Disease and Lung Cancer: A Point of View

Abstract

The goal of this manuscript is to explore the role of clinical proteomics for detecting mutations in chronic obstructive pulmonary disease (COPD) and lung cancer by mass spectrometry-based technology. COPD and lung cancer caused by smoke inhalation are most likely linked by challenging the immune system via partly shared pathways. Genome-wide association studies have identified several single nucleotide polymorphisms which predispose an increased susceptibility to COPD and lung cancer. In lung cancer, this leads to coding mutations in the affected tissues, development of neoantigens, and different functionality and abundance of proteins in specific pathways. If a similar reasoning can also be applied in COPD will be discussed. The technology of mass spectrometry has developed into an advanced technology for proteome research detecting mutated peptides or proteins and finding relevant molecular mechanisms that will enable predicting the response to immunotherapy in COPD and lung cancer patients.

Keywords: COPD; lung cancer; neoantigens.

Figure 1

a) Primary structure of mutant IDH‐1. b,c) Partial mass spectra of mutated IDH‐1(top) and wild type (WT) IDH1 digested proteins. Partial sequence of mutant …RLVSGWVK | PIIIGHHAYGDQYR | ATDFVVPGPG… Partial sequence wild type …RLVSGWVK | PIIIGR|HAYGDQYR| ATDFVVPGPG… Trypsin cleavage sites are indicated with |. Peptides a and b are peptides from other proteins and they may serve as references for intensity variation observed between various samples.