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<img class="aligncenter" src="https://scx1.b-cdn.net/csz/news/800a/2021/scientists-identify-to.jpg"
alt="Scientists identify Tox2 as a key regulator of TFH immune cells"
title="Fig. 1. Tonsillar GC TFH cells express abundant Tox2 and positively correlates with BCL6 and PDCD1.(A) Three tonsillar CD4+ T cell populations were defined according to the expression of ICOS and CXCR5: CXCR5hiICOShi as GC TFH, CXCR5loICOSlo as PreTFH, and CXCR5−ICOS− as naïve CD4. (B) mRNA expression of TOX, TOX2, and TFH-related genes assessed by NanoString in human tonsillar CD4+ T cell subsets. *P < 0.05, ***P < 0.005, ****P < 0.001. (C) Flow RNA analysis of TOX2 in human tonsillar CD4+ T cell subsets. (D) Flow RNA analysis of TOX2 and its association with TFH molecules in human tonsillar CD4+ T cells. (E) Correlation between TOX2, 800 mg acyclovir dosage for cold sores TOX, and BCL6 mRNA and TFH-related molecule mRNA, indicated by Pearson R values. (F) Correlation of TOX2 mRNA with PDCD1 and BCL6 mRNA in tonsillar CD4+ T cell populations. Pearson R values are shown. (G) Expression of Tox2 and Bcl6 proteins in tonsillar CD4+ T cell populations and B cell populations was assessed by Western blotting. Equal amounts of protein were loaded. (H) Localization of Tox2-expressing cells (red) and T cells (green) was analyzed by immunohistochemistry using a frozen tonsil section. White arrow indicates Tox2+ TFH cells in GCs. ns, not significant. Credit: 10.1126/sciadv.abj1249″ width=”800″ height=”530″>
Vaccines have been a mainstay in modern medicine since the late 18th Century, but there is evidence that societies have been using them for more than a thousand years. Throughout this time, all vaccines have operated by activating various immune cells against an infection. A new study in Science Advances led by ASHBi Professor Hideki Ueno reports how the transcription factor Tox2 controls the activation of one of these cells, TFH cells.
One of the most effective ways by which the body fights off an infection is by producing antibodies. Antibodies are not easy to make in the lab, but vaccines stimulate antibody production in the body for a specific infection, such as SARS-CoV-2, the virus responsible for the COVID-19 pandemic.
A number of immune cells are involved in the antibody production, including TFH cells, or T follicular helper cells.
“TFH cells are essential for producing high-affinity antibodies and for generating long-lived antibody-producing cells,” said Ueno. In other words, although TFH cells themselves do not make antibodies, their function heavily influences the immune cells that do. In fact, a number of antibody disorders are associated with their dysfunction.
Reaffirming the importance these cells have in combating infection, or adaptive immunity, is their presence in blood even decades after a vaccination, evidence of them having immunological memory, which describes the ability to promptly react when encountering a pathogen for the second time. Understanding the molecules that enable this persistence, argues Ueno, will benefit vaccine research.
“The molecular mechanism associated with the sustained TFH cell response is unclear. We found that the expression of Tox2 is important,” he said.
Tox2 is recognized for its contribution in immune cell exhaustion; immune cell exhaustion is a discovery that led to Kyoto University Professor Tasaku Honjo winning the Nobel prize in 2018. Cell exhaustion is a natural effect that prevents autoimmune diseases from occurring, but also allows cancers to persist.
The new study found, however, that Tox2 has a very different effect in TFH cells.
“Our study shows that Tox2 is important for the long-term survival and functional maintenance of TFH cells. This suggests a role distinct from other T cells,” said Ueno.
To test this hypothesis, Ueno and his colleagues did two experiments. In one, they overexpressed Tox2 in human TFH cells. In the other, they prevented its expression in mice.
Normally, human TFH cells transform into other types of immune cells upon an immune stimulation. However, the human TFH cells overexpressing Tox2 were stable.
“TFH cells will spontaneously transform with TCR stimulation because they are not terminally differentiated,” said Ueno. “We found that overexpressing Tox2 insulated the cells from this spontaneous transformation. This finding indicates Tox 2 is important for the persistence of TFH cells.”
In contrast, mice with deficient Tox2 showed low levels of TFH cells in the blood and poor antibody responses to infection.
The experiments suggest that targeting Tox2 could be used therapeutically to modulate TFH cells.
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