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Regulation of the germinal center response by T follicular helper cells and type I interferons

Dahlgren, Madelene LU (2016) In Lund University, Faculty of Medicine Doctoral Dissertation Series 2016:54.
Abstract
The protective effect of most currently available vaccines is dependent on high-affinity antibodies and long lived B cell

memory, which develop within organized structures of secondary lymphoid organs called germinal centers (GCs). GC

formation is supported by T follicular helper (Tfh) cells, a subset of CD4+ T cells that develop in parallel to other effector

T cells and specifically localizes to B cell follicles. The aim for the work presented in this thesis was to define how the GC

response and Tfh cell differentiation are regulated by innate effectors, such as conventional dendritic cells (cDCs) and type

I interferons (IFNs), in response to protein immunization adjuvanted by the... (More)
The protective effect of most currently available vaccines is dependent on high-affinity antibodies and long lived B cell

memory, which develop within organized structures of secondary lymphoid organs called germinal centers (GCs). GC

formation is supported by T follicular helper (Tfh) cells, a subset of CD4+ T cells that develop in parallel to other effector

T cells and specifically localizes to B cell follicles. The aim for the work presented in this thesis was to define how the GC

response and Tfh cell differentiation are regulated by innate effectors, such as conventional dendritic cells (cDCs) and type

I interferons (IFNs), in response to protein immunization adjuvanted by the dsRNA-analogue poly(I:C).

In paper I, we show that Tfh cells and GC B cell responses of the IgG1 isotype can develop normally in the absence of

cDCs when a sufficient amount of antigen, allowing initial T cell priming, is provided. In contrast, the concurrent Th1

cell differentiation is impaired together with a selective loss of IgG2c production. We also find that B cells, monocytes and

possibly plasmacytoid DCs (pDCs) redundantly can prime CD4+ T cells in the absence of cDCs, and thereby support

early expression of the Tfh cell-associated chemokine receptor CXCR5. In paper II we find that type I IFNs predominantly

promote IgG2c+ GC B cell differentiation and in this context function through both B cell intrinsic and extrinsic signaling.

While we provide evidence for that direct IFN-γ signaling in B cells controls switching to IgG2c, our results indicate that

type I IFNs regulate IgG2c-associated GC responses beyond isotype switching, as the magnitude of the GC B cell response

is reduced when type I IFNs, but not when IFN-γ, are absent. In contrast to IgG2c, switching to IgG1 is unaffected by

type I IFN deficiency, although the overall magnitude and quality of the IgG1 response also is affected when type I IFN

signaling is abrogated. Additionally, the formation of B cell memory appears to be impaired in the absence of type I IFNs.

In paper III, we demonstrate how clonal competition selectively affects Tfh cell differentiation, GC responses and

generation of IgG1+ GC B cells, while the generation of IgG2c+ GC B cells appears to be less affected.

Taken together, the work included in this thesis increase our understanding of how GC B cell responses and Tfh cell

development are regulated, and furthermore, it suggests that switching to IgG1 and IgG2c associated GC B cell fate

commitment may be differentially dependent on Tfh cells. (Less)
Please use this url to cite or link to this publication:
author
supervisor
opponent
  • Professor Gray, David
organization
publishing date
type
Thesis
publication status
published
subject
keywords
Germinal Center, T follicular helper cell, type I interferon, dendritic cell, adjuvant, differentiation, IgG
in
Lund University, Faculty of Medicine Doctoral Dissertation Series
volume
2016:54
publisher
Faculty of Medicine, Lund University
defense location
Belfrage salen, BMC D15, Sölvegatan 19, Lund
defense date
2016-04-22 13:00
ISSN
1652-8220
ISBN
978-91-7619-280-1
language
English
LU publication?
yes
id
faf247fa-0d49-4e1b-9a0c-cf9494d42157 (old id 8871177)
date added to LUP
2016-04-18 13:02:00
date last changed
2016-09-19 08:45:20
@phdthesis{faf247fa-0d49-4e1b-9a0c-cf9494d42157,
  abstract     = {The protective effect of most currently available vaccines is dependent on high-affinity antibodies and long lived B cell<br/><br>
memory, which develop within organized structures of secondary lymphoid organs called germinal centers (GCs). GC<br/><br>
formation is supported by T follicular helper (Tfh) cells, a subset of CD4+ T cells that develop in parallel to other effector<br/><br>
T cells and specifically localizes to B cell follicles. The aim for the work presented in this thesis was to define how the GC<br/><br>
response and Tfh cell differentiation are regulated by innate effectors, such as conventional dendritic cells (cDCs) and type<br/><br>
I interferons (IFNs), in response to protein immunization adjuvanted by the dsRNA-analogue poly(I:C).<br/><br>
In paper I, we show that Tfh cells and GC B cell responses of the IgG1 isotype can develop normally in the absence of<br/><br>
cDCs when a sufficient amount of antigen, allowing initial T cell priming, is provided. In contrast, the concurrent Th1<br/><br>
cell differentiation is impaired together with a selective loss of IgG2c production. We also find that B cells, monocytes and<br/><br>
possibly plasmacytoid DCs (pDCs) redundantly can prime CD4+ T cells in the absence of cDCs, and thereby support<br/><br>
early expression of the Tfh cell-associated chemokine receptor CXCR5. In paper II we find that type I IFNs predominantly<br/><br>
promote IgG2c+ GC B cell differentiation and in this context function through both B cell intrinsic and extrinsic signaling.<br/><br>
While we provide evidence for that direct IFN-γ signaling in B cells controls switching to IgG2c, our results indicate that<br/><br>
type I IFNs regulate IgG2c-associated GC responses beyond isotype switching, as the magnitude of the GC B cell response<br/><br>
is reduced when type I IFNs, but not when IFN-γ, are absent. In contrast to IgG2c, switching to IgG1 is unaffected by<br/><br>
type I IFN deficiency, although the overall magnitude and quality of the IgG1 response also is affected when type I IFN<br/><br>
signaling is abrogated. Additionally, the formation of B cell memory appears to be impaired in the absence of type I IFNs.<br/><br>
In paper III, we demonstrate how clonal competition selectively affects Tfh cell differentiation, GC responses and<br/><br>
generation of IgG1+ GC B cells, while the generation of IgG2c+ GC B cells appears to be less affected.<br/><br>
Taken together, the work included in this thesis increase our understanding of how GC B cell responses and Tfh cell<br/><br>
development are regulated, and furthermore, it suggests that switching to IgG1 and IgG2c associated GC B cell fate<br/><br>
commitment may be differentially dependent on Tfh cells.},
  author       = {Dahlgren, Madelene},
  isbn         = {978-91-7619-280-1},
  issn         = {1652-8220},
  keyword      = {Germinal Center,T follicular helper cell,type I interferon,dendritic cell,adjuvant,differentiation,IgG},
  language     = {eng},
  publisher    = {Faculty of Medicine, Lund University},
  school       = {Lund University},
  series       = {Lund University, Faculty of Medicine Doctoral Dissertation Series},
  title        = {Regulation of the germinal center response by T follicular helper cells and type I interferons},
  volume       = {2016:54},
  year         = {2016},
}