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Viral superantigen drives extrafollicular and follicular B cell differentiation leading to virus-specific antibody production.

Luther SA, Gulbranson-Judge A, Acha-Orbea H, MacLennan IC - J. Exp. Med. (1997)

Bottom Line: The response to MMTV(SW) in draining lymph nodes was compared with the response to haptenated chicken gamma globulin (NP-CGG) using flow cytometry and immunohistology.Germinal centers develop in both responses, but those induced by MMTV(SW) appear later and are smaller.Most T cells activated in the T zone and germinal centers in the MMTV(SW) response are superantigen specific and these persist for weeks in lymph nodes draining the site MMTV(SW) injection: this contrasts with the selective loss of superantigen-specific T cells from other secondary lymphoid tissues.

View Article: PubMed Central - PubMed

Affiliation: Ludwig Institute for Cancer Research, University of Lansanne, Epalinges.

ABSTRACT
Mouse mammary tumor virus (MMTV[SW]) encodes a superantigen expressed by infected B cells. It evokes an antibody response specific for viral envelope protein, indicating selective activation of antigen-specific B cells. The response to MMTV(SW) in draining lymph nodes was compared with the response to haptenated chicken gamma globulin (NP-CGG) using flow cytometry and immunohistology. T cell priming occurs in both responses, with T cells proliferating in association with interdigitating dendritic cells in the T zone. T cell proliferation continues in the presence of B cells in the outer T zone, and B blasts then undergo exponential growth and differentiation into plasma cells in the medullary cords. Germinal centers develop in both responses, but those induced by MMTV(SW) appear later and are smaller. Most T cells activated in the T zone and germinal centers in the MMTV(SW) response are superantigen specific and these persist for weeks in lymph nodes draining the site MMTV(SW) injection: this contrasts with the selective loss of superantigen-specific T cells from other secondary lymphoid tissues. The results indicate that this viral superantigen, when expressed by professional antigen-presenting cells, drives extrafollicular and follicular B cell differentiation leading to virus-specific antibody production.

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Quantitative analysis  of T and B cell subsets within the  draining popliteal LN responding to MMTV(SW) (a, c), or  alum-precipitated NP-CGG plus  B. pertussis (b, d). Cell suspensions were analyzed by flow cytometry as in Fig. 2. Values in a  and b represent mean numbers of  cells/node in different CD4+,  Vβ subsets and those in c and d  mean numbers of CD4−CD8−  cells/node sorted on the basis of  their expression of IgD and  B220. The same control responses were included as for Fig.  2. Three mice were analyzed for  each immunization at each timepoint.
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Figure 4: Quantitative analysis of T and B cell subsets within the draining popliteal LN responding to MMTV(SW) (a, c), or alum-precipitated NP-CGG plus B. pertussis (b, d). Cell suspensions were analyzed by flow cytometry as in Fig. 2. Values in a and b represent mean numbers of cells/node in different CD4+, Vβ subsets and those in c and d mean numbers of CD4−CD8− cells/node sorted on the basis of their expression of IgD and B220. The same control responses were included as for Fig. 2. Three mice were analyzed for each immunization at each timepoint.

Mentions: BALB/c mice were injected into both hind footpads with milk-purified infectious MMTV(SW) or alum-precipitated NP-CGG with killed B. pertussis microorganisms. The specific serum antibody titers of these immunized mice were measured and the immune responses in the draining popliteal LN were compared. To assess the proliferative response, mice were given a pulse of BrdU i.p. 2.5 h before death to identify and localize cells that had been in S phase of the cell cycle over this period. One draining popliteal LN was used to quantify cellular subsets by flow cytometry; the contralateral draining LN was used to colocalize these subsets by immunohistology. With both methods, cells were stained for cell differentiation and proliferation markers between day 0 and day 30 after antigen challenge. The antibody responses are shown in Fig. 1, while the flow cytometry data are shown in Figs. 2 and 4 and the histological analyses in Figs. 3, 5, 6, 7.


Viral superantigen drives extrafollicular and follicular B cell differentiation leading to virus-specific antibody production.

Luther SA, Gulbranson-Judge A, Acha-Orbea H, MacLennan IC - J. Exp. Med. (1997)

Quantitative analysis  of T and B cell subsets within the  draining popliteal LN responding to MMTV(SW) (a, c), or  alum-precipitated NP-CGG plus  B. pertussis (b, d). Cell suspensions were analyzed by flow cytometry as in Fig. 2. Values in a  and b represent mean numbers of  cells/node in different CD4+,  Vβ subsets and those in c and d  mean numbers of CD4−CD8−  cells/node sorted on the basis of  their expression of IgD and  B220. The same control responses were included as for Fig.  2. Three mice were analyzed for  each immunization at each timepoint.
© Copyright Policy
Related In: Results  -  Collection

Show All Figures
getmorefigures.php?uid=PMC2196032&req=5

Figure 4: Quantitative analysis of T and B cell subsets within the draining popliteal LN responding to MMTV(SW) (a, c), or alum-precipitated NP-CGG plus B. pertussis (b, d). Cell suspensions were analyzed by flow cytometry as in Fig. 2. Values in a and b represent mean numbers of cells/node in different CD4+, Vβ subsets and those in c and d mean numbers of CD4−CD8− cells/node sorted on the basis of their expression of IgD and B220. The same control responses were included as for Fig. 2. Three mice were analyzed for each immunization at each timepoint.
Mentions: BALB/c mice were injected into both hind footpads with milk-purified infectious MMTV(SW) or alum-precipitated NP-CGG with killed B. pertussis microorganisms. The specific serum antibody titers of these immunized mice were measured and the immune responses in the draining popliteal LN were compared. To assess the proliferative response, mice were given a pulse of BrdU i.p. 2.5 h before death to identify and localize cells that had been in S phase of the cell cycle over this period. One draining popliteal LN was used to quantify cellular subsets by flow cytometry; the contralateral draining LN was used to colocalize these subsets by immunohistology. With both methods, cells were stained for cell differentiation and proliferation markers between day 0 and day 30 after antigen challenge. The antibody responses are shown in Fig. 1, while the flow cytometry data are shown in Figs. 2 and 4 and the histological analyses in Figs. 3, 5, 6, 7.

Bottom Line: The response to MMTV(SW) in draining lymph nodes was compared with the response to haptenated chicken gamma globulin (NP-CGG) using flow cytometry and immunohistology.Germinal centers develop in both responses, but those induced by MMTV(SW) appear later and are smaller.Most T cells activated in the T zone and germinal centers in the MMTV(SW) response are superantigen specific and these persist for weeks in lymph nodes draining the site MMTV(SW) injection: this contrasts with the selective loss of superantigen-specific T cells from other secondary lymphoid tissues.

View Article: PubMed Central - PubMed

Affiliation: Ludwig Institute for Cancer Research, University of Lansanne, Epalinges.

ABSTRACT
Mouse mammary tumor virus (MMTV[SW]) encodes a superantigen expressed by infected B cells. It evokes an antibody response specific for viral envelope protein, indicating selective activation of antigen-specific B cells. The response to MMTV(SW) in draining lymph nodes was compared with the response to haptenated chicken gamma globulin (NP-CGG) using flow cytometry and immunohistology. T cell priming occurs in both responses, with T cells proliferating in association with interdigitating dendritic cells in the T zone. T cell proliferation continues in the presence of B cells in the outer T zone, and B blasts then undergo exponential growth and differentiation into plasma cells in the medullary cords. Germinal centers develop in both responses, but those induced by MMTV(SW) appear later and are smaller. Most T cells activated in the T zone and germinal centers in the MMTV(SW) response are superantigen specific and these persist for weeks in lymph nodes draining the site MMTV(SW) injection: this contrasts with the selective loss of superantigen-specific T cells from other secondary lymphoid tissues. The results indicate that this viral superantigen, when expressed by professional antigen-presenting cells, drives extrafollicular and follicular B cell differentiation leading to virus-specific antibody production.

Show MeSH
Related in: MedlinePlus