Recurring patterns in patient accounts suggest the existence of an inverse relationship between personal history of infectious fever and cancer risk, and these patterns are documented throughout decades of medical literature. However, evidence supporting this correlation continues to be primarily anecdotal. In “Toward Antitumour Immunity and Febrile Infections: Gamma/Delta (γδ) T Cells Hypothesis” published in The Quarterly Review of Biology, Wieslaw Kozak, Tomasz Jedrzejewski, Malgorzata Pawlikowska, Jakub Piotrowski, and Sylwia Wrotek propose a mechanistic hypothesis that focuses on the potential impact infectious fever has on a particular subset of T cells, known as gamma/delta (gd) T cells.
Drawing upon previous research and experimental data, the authors argue that repeated exposure to fever enhances the ability of gd T cells to detect cellular abnormalities and to foster inhospitable environments that destroy malignant cells. This paper is the first to acknowledge the role that gd T cells may play as participants in this inverse relationship.
Infectious fever is the defensive and adaptive reaction that occurs when an organism’s immune system comes into contact with exogenous pyrogens, or pathogen-associated molecular pattern (PAMP). Upon recognition of these exogenous pyrogens, endogenous mediators — also known as endogenous pyrogens — engage the febrile system. According to previous work by Shephard et al., a febrile system is composed of all of the mechanisms responsible for facilitating a fever as well as the various systems the fever affects. Thermoregulatory mechanisms are activated, resulting in the elevation of an organism’s core body temperature.
The authors further elaborate on the function of endogenous mediators, like cytokines.
“In short, endogenous mediators of fever redirect metabolic substrates and energy to the immune system during fever. This markedly enhances the frequency of a vast range of immune effectors, including lymphocytes expressing gd heterodimer receptors, which possess a potent anti-infectious and antitumour competence,” the authors write.
Gamma/delta T cells possesses receptors (TCRs) comprised of gamma/delta chain heterodimer. In fact, the authors posit that the unique attributes of gd T lymphocytes — lower TCR variability, fewer gene segment rearrangements, and TCRs with older evolutionary memory — enable the cells to enact processes that aid in decreasing cancer risk, such as immune surveillance and attacking cancerous cells. Vg9Vd2 T cells are capable of responding to various types of cancer, such as carcinoma, lymphoma, prostate, myeloma, and sarcoma. Exposure to infection significantly expands the quantity of gd T cells. During infection, blood Vg9Vd2 T cells can increase in number until they constitute 60 percent of the total amount of lymphocytes.
While previous research and current cancer immunotherapy practices predominately focus on alpha/beta (ab) T cells, analysis of the interaction between fever and gd T cells may generate further inquiry into the larger impact and the clinical benefits of this relationship.
Paper: Wieslaw Kozak, Tomasz Jedrzejewski, Malgorzata Pawlikowska, Jakub Piotrowski, Sylwia Wrotek. Toward Antitumour Immunity and Febrile Infections: Gamma/Delta (γδ) T Cells Hypothesis. The Quarterly Review of Biology, 2018; 93 (3): 187 DOI: 10.1086/699409