Follicular B helper T cells

Follicular B helper T cells (also known as just follicular helper T cells or TFH), are antigen-experienced CD4+ T cells found in the periphery within B cell follicles of secondary lymphoid organs such as lymph nodes, spleens and Peyer's patches, and are identified by their constitutive expression of the B cell follicle homing receptor CXCR5.[1] Upon cellular interaction and cross-signaling with their cognate follicular (Fo B) B cells, TFH cells trigger the formation and maintenance of germinal centers through the expression of CD40 ligand (CD40L) and the secretion of IL-21[2] and IL-4.[3] TFH cells also migrate into these seeded germinal centers, predominantly composed of rapidly dividing and mutating B cells. Within germinal centers, TFH cells play a critical role in mediating the selection and survival of B cells that go on to differentiate either into special plasma cells capable of producing high affinity antibodies against foreign antigen, and memory B cells capable of quick immune re-activation in the future if ever the same antigen is re-encountered. TFH cells are also thought to facilitate negative selection of potentially autoimmune-causing mutated B cells in the germinal center. However, the biomechanisms by which TFH cells mediate germinal center tolerance are yet to be fully understood.

It is possible that TFH cells might arise as branches in the Th1 and Th2 differentiation pathways but their precise lineage relationship to the other effector CD4+ T cell subsets is still uncertain. Recent studies have however shown that TFH have distinct gene expression profiles, supporting the theory that TFH are a subset of CD4+ T cells distinct from Th-1, Th-2, Th-17 or Tregs.[4][5]

The function of TFH cells.
A subset of naive T cells in the T cell zone are activated by antigen and migrate to the follicles where they differentiate into TFH cells that interact with and instruct Follicular B (Fo B) cells to undergo isotype switching, somatic hypermutation, and rapid cellular division to seed germinal centers (GC). Within these germinal centers, TFH cells continue to provide help to GC B cells to facilitate their production of high affinity antibody producing plasma cells (PC) and long-lived memory (Mem) B cells.

Biomolecular characterization

The inducible T-cell co-stimulator (CD278 or ICOS) is proven to provide a particularly critical signal for TFH cells since experimental mice deficient in ICOS are unable to develop any TFH.[6] Additionally, it has been shown that ICOS induces the secretion of IL-21 cytokine by activated CD4+ T cells and that IL-21 plays a crucial role in the development of TFH cells and germinal centers.[7][8] Also Bcl-6 is a transcription factor identified in TFH cells, but it may have roles that extend beyond this subset, because it has also been implicated in memory CD8+ T cell development.[9]

In germinal centers, antigen-experienced TFH cells rapidly upregulate the expression of CD40L, which binds and stimulates the B cell surface receptor CD40.[10] TFH cell-dependent paracrine activation of B cell CD40 results in B cell survival and differentiation, including the induction of AID (activation-induced (cytidine) deaminase).[11] AID expression (encoded by the AICDA gene) causes B cell antibodies to class switch from IgM/IgD to other antibody isotypes and drives somatic hypermutation during clonal proliferation. The switched antibodies acquire better effector functions, and hypermutated antibody shows greater affinity for antigen.

Classes of TFH cells

TFH cells formed early in the nascent stages of a germinal center reaction are formally called pre-TFH cells. They are uniquely found predominantly at the border of the T cell zone that merges with the B cell follicles and germinal centers. Pre-TFH cells are functionally very similar to other TFH cells in facilitating germinal center B cell reactions however, in addition, they are also capable of driving follicular B cell development adjacent to and outside of germinal centers to produce quickly responsive but non-durable plasma cell-driven antibody responses (known as the extrafollicular response).

Those TFH cells specifically residing within a mature germinal center are sometimes referred to as GC TFH cells (for Germinal Center TFH cells) to distinguish them from pre-TFH cells.[12][13] There is also a minor sub-class within this population of GC Tfh cells that express the gene Foxp3, encoding for a transcription factor. This small discrete sub-population of cells, called TFR cells (for T Follicular Regulatory cells), are important in helping to control and limit the magnitude of normal germinal center responses such that they avoid the potential to produce abnormally mutated or self-reactive autoimmune-associated antibodies.[14] Therefore, TFR cells are a uniquely inhibitory influence during a germinal center reaction.

Medical relevance

Generating lasting immune memory

TFH cells are considered an indispensable T cell subset in the generation and maintenance of germinal center responses. Therefore, in the absence of TFH cells, similar to B cell activation by T-cell independent antigens, a quick burst of low affinity plasma cell production is formed but this does not lead to germinal center induction nor permit antibody affinity maturation or the differentiation of effective memory B cells which are essential in fortifying the body against subsequent infections. Specifically, germinal center-dependent memory B cells are the drivers of recall antibody production during a secondary immune response. Therefore, the proper activation and development of TFH cells is central to the efficacy of immunizations and vaccine design for the induction of long-term immunity. In a Bangladeshi population study of patients infected with Vibrio cholera and healthy human volunteers administered with an existing cholera vaccine,[15] a memory TFH response specifically against cholera antigen had correlated with further antibody production by B cells.

Controlling age-related immune decline

With normal aging comes a gradual diminishing of the body's immune system. This phenomenon called immunosenescence is largely due to a decline of T cell function, including the capacity for TFH cells to properly support germinal center responses.[16] This may be in part due to lower CD40L levels on the cell surface of TFH cells in the aged.[17]

Avoiding autoimmunity

Unchecked or overactive TFH cell immune responses have the potential to mount unwarranted germinal centers, composed of aberrantly mutated B cells that can drive antibody-mediated autoimmune diseases. Elevated levels of TFH-like cells can be detected in the blood of a subset of human patients with systemic lupus erythematosus (SLE) and Sjogren's syndrome.[18] However, scientific evidence suggesting TFH cells can definitively cause autoimmunity in humans remains incomplete.

References

  1. ↑ Fazilleau; Mark, L; McHeyzer-Williams, LJ; McHeyzer-Williams, MG; et al. (March 2009). "Follicular helper T cells: lineage and location". Immunity 30 (3): 324–35. doi:10.1016/j.immuni.2009.03.003. PMC 2731675. PMID 19303387.
  2. ↑ Seo; Youn, J; Kim, PH; et al. (May 2009). "IL-21 ensures TGF-beta 1-induced IgA isotype expression in mouse Peyer's patches". J Leukoc Biol 85 (5): 744–50. doi:10.1189/jlb.0708450. PMID 19168593.
  3. ↑ Zaretsky; Taylor, JJ; King, IL; Marshall, FA; Mohrs, M; Pearce, EJ; et al. (May 2009). "T follicular helper cells differentiate from Th2 cells in response to helminth antigens". J Exp Med 206 (5): 991–9. doi:10.1084/jem.20090303. PMC 2715032. PMID 19380637.
  4. ↑ Chtanova; Tangye, SG; Newton, R; Frank, N; Hodge, MR; Rolph, MS; MacKay, CR; et al. (July 2004). "T follicular helper cells express a distinctive transcriptional profile, reflecting their role as non-Th1/Th2 effector cells that provide help for B cells". J Immunol 173 (1): 68–78. doi:10.4049/jimmunol.173.1.68. PMID 15210760.
  5. ↑ Nurieve; Chung, Y; Hwang, D; Yang, XO; Kang, HS; Ma, L; Wang, YH; Watowich, SS; et al. (July 2008). "Generation of T follicular helper cells is mediated by interleukin-21 but independent of T helper 1, 2, or 17 cell lineages". Immunity 29 (1): 138–49. doi:10.1016/j.immuni.2008.05.009. PMC 2556461. PMID 18599325.
  6. ↑ Akiba; Takeda, K; Kojima, Y; Usui, Y; Harada, N; Yamazaki, T; Ma, J; Tezuka, K; et al. (Aug 2005). "The role of ICOS in the CXCR5+ follicular B helper T cell maintenance in vivo". J Immunol 175 (4): 2340–8. doi:10.4049/jimmunol.175.4.2340. PMID 16081804.
  7. ↑ Bauquet; Jin, H; Paterson, AM; Mitsdoerffer, M; Ho, IC; Sharpe, AH; Kuchroo, VK (Feb 2009). "The costimulatory molecule ICOS regulates the expression of c-Maf and IL-21 in the development of follicular T helper cells and TH-17 cells". Nat Immunol 10 (2): 167–75. doi:10.1038/ni.1690. PMC 2742982. PMID 19098919.
  8. ↑ Vogelzang; McGuire, HM; Yu, D; Sprent, J; MacKay, CR; King, C (July 2008). "A fundamental role for interleukin-21 in the generation of T follicular helper cells". Immunity 29 (1): 127–37. doi:10.1016/j.immuni.2008.06.001. PMID 18602282.
  9. ↑ Ichii; Sakamoto, A; Hatano, M; Okada, S; Toyama, H; Taki, S; Arima, M; Kuroda, Y; Tokuhisa, T; et al. (June 2002). "Role for Bcl-6 in the generation and maintenance of memory CD8+ T cells". Nat Immunol 3 (6): 558–63. doi:10.1038/ni802. PMID 12021781.
  10. ↑ Kim, JR; Lim, HW; Kang, SG; Hillsamer, P; Kim, CH (Feb 4, 2005). "Human CD57+ germinal center-T cells are the major helpers for GC-B cells and induce class switch recombination.". BMC immunology 6: 3. doi:10.1186/1471-2172-6-3. PMC 548684. PMID 15694005.
  11. ↑ McHeyzer-Williams, M; Okitsu, S; Wang, N; McHeyzer-Williams, L (Dec 9, 2011). "Molecular programming of B cell memory.". Nature reviews. Immunology 12 (1): 24–34. doi:10.1038/nri3128. PMC 3947622. PMID 22158414.
  12. ↑ Yusuf I, Kageyama R, Monticelli L, Johnston RJ, Ditoro D, Hansen K, Barnett B, Crotty S. (July 2010). "Germinal center T follicular helper cell IL-4 production is dependent on signaling lymphocytic activation molecule receptor (CD150).". J. Immunol. 185 (1): 190–202. doi:10.4049/jimmunol.0903505. PMC 2913439. PMID 20525889.
  13. ↑ Ramiscal RR, Vinuesa CG. (March 2013). "T-cell subsets in the germinal center.". Immunol. Rev. 252 (1): 146–55. doi:10.1111/imr.12031. PMID 23405902.
  14. ↑ Wollenberg I1, Agua-Doce A, Hernández A, Almeida C, Oliveira VG, Faro J, Graca L. (November 2011). "Regulation of the germinal center reaction by Foxp3+ follicular regulatory T cells.". J. Immunol. 187 (9): 4553–60. doi:10.4049/jimmunol.1101328. PMID 21984700.
  15. ↑ Arifuzzaman, M; Rashu, R; Leung, DT; Hosen, MI; Bhuiyan, TR; Bhuiyan, MS; Rahman, MA; Khanam, F; Saha, A; Charles, RC; LaRocque, RC; Weil, AA; Clements, JD; Holmes, RK; Calderwood, SB; Harris, JB; Ryan, ET; Qadri, F (August 2012). "Antigen-specific memory T cell responses after vaccination with an oral killed cholera vaccine in Bangladeshi children and comparison to responses in patients with naturally acquired cholera.". Clinical and vaccine immunology : CVI 19 (8): 1304–11. doi:10.1128/CVI.00196-12. PMC 3416086. PMID 22739692. Cite uses deprecated parameter |coauthors= (help)
  16. ↑ Lefebvre JS, Maue AC, Eaton SM, Lanthier PA, Tighe M, Haynes L. (2012). "The aged microenvironment contributes to the age-related functional defects of CD4 T cells in mice.". Aging Cell 11 (5): 732–40. doi:10.1111/j.1474-9726.2012.00836.x. PMC 3444657. PMID 22607653.
  17. ↑ Perkey E, Miller RA, Garcia GG. (2012). "Ex vivo enzymatic treatment of aged CD4 T cells restores cognate T cell helper function and enhances antibody production in mice.". J Immunol 189 (12): 5582–9. doi:10.4049/jimmunol.1200487. PMC 3518580. PMID 23136198.
  18. ↑ Craft JE. (2012). "Follicular helper T cells in immunity and systemic autoimmunity.". Nat Rev Rheumatol. 8 (6): 337–47. doi:10.1038/nrrheum.2012.58. PMC 3604997. PMID 22549246.
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