A fate determination fork-in-the-road for germinal center Tfh and T memory cells

Some PD-1+CXCR5+CD4+ T cells will become germinal center-Tfh cells that are essential for B cells to become high-affinity antibody-producing cells. Others do not take that path, instead becoming memory T cells.

1205243772681563.cZLjRGDczqL7jxQkTRxB height640Fangming Zhu,
Photography: Steve Wood
Follicular helper T cells, or Tfh cells, have a crucial role in immune defense. Without Tfh cells, B cells cannot form germinal center, or GC, responses during which high-affinity antibodies are generated.

When naïve CD4-positive CD4+ T cells receive news of an infection elsewhere in the body, they become activated with additional cell-surface markers, and they differentiate in two directions, becoming either PD-1+CXCR5­– or PD-1+CXCR5+ T cells. PD-1 and CXCR5 are two different cell-surface markers, and the plus and minus signs tell whether they are present or absent.

The PD-1+CXCR5+CD4+ T cells have the capacity to differentiate, move into B-cell follicles and mature into GC-Tfh cells. These GC-Tfh cells are essential for the formation of germinal centers, the place where B cells generate high-affinity antibodies.

But there was a mystery about these PD-1+CXCR5+CD4+ T cells. While some PD-1+CXCR5+CD4+ cells enter the follicle, others do not. Now Hui Hu, Ph.D., and colleagues at the University of Alabama at Birmingham have identified a cell-surface marker that indicates which T cells will go into the follicles and which ones will stay out. A sustained appearance of the cell-surface protein, Tigit, identifies the Tigit-positive PD-1+CXCR5+CD4+ T cells, or pre-Tfh, that will become GC-Tfh cells, they report in a study published in Nature Communications.

“Which of the PD-1+CXCR5+CD4+ T cells will differentiate into PD-1hiCXCR5hi GC-Tfh cells while the others have a different fate is a long-standing question in the Tfh field,” said Hu, an associate professor in the UAB Department of Microbiology.

Importantly, the Tigit-negative PD-1+CXCR5+CD4+ T cells are found to be the precursors to long-lived memory CXCR5+CD4+ T cells that will quickly awaken the immune response to a later infection by the same pathogen. 

1205243772681565.GyuMQUrPoTKUWith4Gt8 height640Ryan McMonigle, M.D., Ph.D.,
Photography: Steve Wood
Hu and co-first authors Fangming Zhu, and Ryan J. McMonigle, M.D., Ph.D., UAB Department of Microbiology, also looked into this formation of memory T cells. It has been observed that the surface marker CCR7 is re-expressed in CXCR5+CD4+ T memory cells rather than CXCR5–CD4+ T memory cells, leading to the recognition by some of CCR7+CXCR5+CD4+ T cells as central memory CD4+ T cells.

“In our study, using both influenza virus infection and protein immunization models, we have discovered conditions under which CCR7 and CD62L can be biased to CXCR5+ T cells or equally expressed between CXCR5–CD4+ T memory cells and CXCR5+CD4+ T memory cells,” Hu said. Hu and colleagues found that the strength of the T cell response — as influenced by the competition within the local environment and the location in the draining versus non-draining secondary lymphoid organs — and the type of challenge, viral infection or antigen immunization, play critical roles in determining the central memory phenotype of CD4+ T cells.

“Given the historical context and the current controversy surrounding CXCR5+ ‘central memory’ CD4+ T cells, and also the differences between CXCR5–CD4+ T cells and CXCR5+CD4+ T cells, our findings will prompt the field to reassess how we describe the different memory CD4+ T cells,” Hu said. “To what extent that GC-Tfh cells give rise to memory CXCR5+CD4+ T cells is also an open question,” Hu added. 

Numerous previous studies and many current studies still do not separate PD-1+CXCR5+Bcl6+ pre-Tfh cells from PD-1hiCXCR5hiBcl6hi germinal center-Tfh cells, Hu says. The UAB researchers also showed that pre-Tfh cells undergo extended differentiation in transition to GC-Tfh cells, as seen in substantial changes in differential gene expression — where genes are either activated or turned off. They also found differences in chromatin accessibility during differentiation — where the packaging of DNA in the chromosome is loosened to allow gene expression.

“Importantly, we found that c-Maf, a transcription factor that has been reported to be involved in Tfh cell differentiation, exerts a critical function specifically in the transition step from pre-Tfh cells to GC-Tfh cells,” Hu said. “More excitingly, we have identified Plekho1, a c-Maf downstream factor, as a novel regulator that plays stage-specific roles in GC-Tfh cell differentiation.”

1205243772681567.wQFOeyWo35DpUoH0vcYr height640Hui Hu, Ph.D.,
Photography: Lexi Coon
“Our study has clarified several important but controversial points in Tfh cell differentiation and provided compelling evidence to elucidate the intricacy of GC-Tfh cell differentiation and the varied CD4+ memory T cells,” Hu said.

These findings have opened many new avenues to study the fundamental mechanisms in Tfh cell differentiation and CD4+ T cell memory, Hu says. How a cell takes on one fate over another and how that fate is maintained is one of the most fundamental questions in biology. Understanding the various stages, cell subsets and the underlying regulatory mechanisms of Tfh cell differentiation can facilitate the design of new strategies to treat infectious diseases and autoimmune disorders and can aid vaccine development for new pandemic threats.

Co-authors with Hu, Zhu and McMonigle in the study, “Spatiotemporal resolution of germinal center Tfh cell differentiation and divergence from central memory CD4+ T cell fate,” are Andrew R. Schroeder, Xianyou Xia, Diego O. Sialer, Yin-Hu Wang, Kelly M. Chandler and Emily R. Brown, UAB Department of Microbiology; David Figge, UAB Department of Pathology; Braxton D. Greer and Olaf Kutsch, UAB Department of Medicine Division of Infectious Diseases; Edahí González-Avalos, La Jolla Institute for Immunology, La Jolla, California; Adam J. Getzler and Matthew E. Pipkin, The Scripps Research Institute, Jupiter, Florida; Changchun Xiao, The Scripps Research Institute, La Jolla, California; and Yohsuke Harada, Tokyo University of Science, Tokyo, Japan. 

This work was supported by National Institutes of Health grants AI130232, AI167986, AI122842, AI116188 and AI133679; NIH training grants AR069516, AI007051 and GM008361; and NIH grant AI027767-26 to the University of Alabama at Birmingham Center for AIDS Research

At UAB, the Marnix E. Heersink School of Medicine is home for the departments of Microbiology, Pathology and Medicine, and the Center for AIDS Research.