Antigen-Specific Stimulation of Human Autoreactive B Lymphocytes

1986 ◽  
pp. 41-44
Author(s):  
T. Logtenberg ◽  
A. Kroon ◽  
F. H. J. Gmelig-Meyling ◽  
R. E. Ballieux
Keyword(s):  
B Lymphocytes ◽  
Specific Stimulation ◽  
Stimulation Of

Stimulation of phosphoinositide signaling pathway in murine B lymphocytes by a novel guanosine analog, 7-thia-8-oxoguanosine

1989 ◽  
Vol 163 (3) ◽  
pp. 1306-1311 ◽  
Author(s):  
Zahra Parandoosh ◽  
Emmanuel Ojo-Amaize ◽  
Roland K. Robins ◽  
Weldon B. Jolley ◽  
Boanerges Rubalcava
Keyword(s):  
Signaling Pathway ◽  
B Lymphocytes ◽  
Phosphoinositide Signaling ◽  
Stimulation Of

scholarly journals T lymphocyte-dependent B lymphocyte proliferative response to antigen. I Genetic restriction of the stimulation of B lymphocyte proliferation.

1981 ◽  
Vol 153 (4) ◽  
pp. 871-882 ◽  
Author(s):  
H Y Tse ◽  
J J Mond ◽  
W E Paul
Keyword(s):  
T Lymphocytes ◽  
B Lymphocytes ◽  
T Lymphocyte ◽  
Lymphocyte Proliferation ◽  
B Lymphocyte ◽  
Antigen Specificity ◽  
Apparent Lack ◽  
The Face ◽  
Stimulation Of

For the purpose of examining more closely the interaction between T and B lymphocytes, we have developed an in vitro T lymphocyte-dependent B lymphocyte proliferation assay. Proliferation of B lymphocytes in response to antigen was found to depend on the presence of primed T lymphocytes; the B lymphocytes could be derived from nonprimed animals. It appears that these B cells were nonspecifically recruited to proliferate. This nonspecific recruitment, however, was found to be Ir-gene restricted in that B lymphocytes from B10.S mice, which are genetic nonresponders to the polymer Glu60-Ala30-Tyr10 (GAT), could not be stimulated by GAT-primed (responder X nonresponder) F1 T cells. The apparent lack of antigen specificity in the face of Ir gene-restricted T-B interaction may have important implications in our understanding of the recognition unit(s) on T lymphocytes.

Antigen-specific stimulation and trans-stimulation of T cells in long-term culture

1979 ◽  
Vol 9 (9) ◽  
pp. 665-670 ◽  
Author(s):  
Andrei A. Augustin ◽  
Michael H. Julius ◽  
Humberto Cosenza
Keyword(s):  
T Cells ◽  
Long Term Culture ◽  
Specific Stimulation ◽  
Stimulation Of

scholarly journals Autologous stimulation of human lymphocyte subpopulation.

1975 ◽  
Vol 142 (5) ◽  
pp. 1327-1333 ◽  
Author(s):  
G Opelz ◽  
M Kiuchi ◽  
M Takasugi ◽  
P I Terasaki
Keyword(s):  
T Cells ◽  
B Cells ◽  
B Lymphocytes ◽  
Human Lymphocyte ◽  
Lymphocyte Subpopulation ◽  
High Background ◽  
Background Stimulation ◽  
Most Probable Explanation ◽  
Stimulation Of

The background stimulation universally seen when lymphocytes are cultured in vitro has been shown to be markedly lowered by reducing the proportion of B lymphocytes. B-rich fractions of lymphocytes had extremely high background stimulation. It is concluded that stimulation of T cells, probably by autologous B cells, provides the most probable explanation for the findings described.

scholarly journals On the Non-Specific Stimulation of Agglutinins. With Especial Reference to the Enteric Fevers and Typhus Fever

1929 ◽  
Vol 28 (4) ◽  
pp. 418-448 ◽  
Author(s):  
A. Felix
Keyword(s):  
Qualitative Method ◽  
Published Data ◽  
Enteric Infection ◽  
Widal Test ◽  
Enteric Infections ◽  
The Difference ◽  
Specific Stimulation ◽  
Enteric Group ◽  
Typhus Fever ◽  
Stimulation Of

(1) The review of the published data furnishes additional evidence in support of the view that no technique whatsoever, Dreyer's technique included, based on the quantitative method of the agglutination reaction hitherto used, is capable of affording a differentiation between inoculation and infection agglutinins.(2) These techniques are concerned always exclusively in the demonstration of the labilotropic H agglutinins ofB. typhosusandB. paratyphosusA. and B. and it is the behaviour of these agglutinins that is the responsible factor in producing the phenomena.(3) In various febrile conditions in inoculated individuals these H agglutinins undergo a re-stimulation resulting in a curve of agglutination which is indistinguishable from that due to specific stimulation. The re-stimulation of the labilotropic inoculation agglutinins is of the same nonspecific character (i.e.heterologous) in the course of enteric infections as in the course of other febrile diseases.(4) The observation of this non-specific re-stimulation is independent of the technique used; living bacilli and suspensions preserved with phenol or formalin (Dreyer's technique included) do not in this respect behave differently.(5) The proposed qualitative method for the Widal test depends, in inoculated individuals, exclusively upon the behaviour of the stabilotropic O agglutinins. In their presence it is capable of affording the certain diagnosis of an enteric infection; in their absence the negative result of the test is not conclusive; if T.A.B. vaccine has been used it is only possible to diagnose enteric group without being able to differentiate typhoid from paratyphoid A. or B.; if T. vaccine has been used then A. or B. infection can be differentiated but not T.(1) The conclusions previously arrived at by means of the qualitative method of the Widal test were fully confirmed. By eliminating the labilotropic H agglutinins from any consideration—in the case of previously sensibilised individuals—agglutination due to the specific stimulation in active enteric infection can be distinguished definitely from that due to the nonspecific re-stimulation by various febrile diseases.(2) Normal and immune O agglutinins forB. typhosusandB. paratyphosusA. and B., as well as those forB. proteusX 19, are not liable to non-specific stimulation in the course of various febrile diseases.(3) One more of the supposed differences in nature between the Widal test and the Weil-Felix test is thereby eliminated.(4) The difference in the response to non-specific stimulation shown to exist in stabilotropic and labilotropic agglutination seems more likely to be one of degree than one in nature and needs further investigation.

scholarly journals Protection of C57BL/10 mice by vaccination with association of purified proteins from Leishmania (Leishmania) amazonensis

1999 ◽  
Vol 41 (4) ◽  
pp. 243-248 ◽  
Author(s):  
Ana Mariela MORA ◽  
Wilson MAYRINK ◽  
Roberto Teodoro da COSTA ◽  
Carlos Alberto da COSTA ◽  
Odair GENARO ◽  
...  
Keyword(s):  
Cutaneous Leishmaniasis ◽  
Crude Extract ◽  
Gel Electrophoresis ◽  
Protective Immunity ◽  
Polyacrylamide Gel Electrophoresis ◽  
Challenge Infection ◽  
Leishmania Amazonensis ◽  
The Past ◽  
Specific Stimulation ◽  
Stimulation Of

In the past few years, induction of protective immunity to cutaneous leishmaniasis has been attempted by many researchers using a variety of antigenic preparations, such as living promastigotes or promastigote extracts, partially purified, or defined proteins. In this study, eleven proteins from Leishmania (Leishmania) amazonensis (LLa) with estimated molecular mass ranging from 97 to 13.5kDa were isolated by polyacrylamide gel electrophoresis and electro-elution. The proteins were associated as vaccine in different preparations with gp63 and BCG (Bacilli Calmette-Guérin). The antigenicity of these vaccines was measured by their ability to induce the production of IFN-<FONT FACE="Symbol">g</font> by lymphocyte from subjects vaccinated with Leishvacin<FONT FACE="Symbol">â</font> . The immunogenicity was evaluated in vaccinated mice. C57BL/10 mice were vaccinated with three doses of each vaccine consisting of 30 <FONT FACE="Symbol">m</font>g of each protein at 15 days interval. One hundred <FONT FACE="Symbol">m</font>g of live BCG was only used in the first dose. Seven days after the last dose, they received a first challenge infection with 105 infective promastigotes and four months later, a second challenge was done. Two months after the second challenge, 42.86% of protection was obtained in the group of mice vaccinated with association of proteins of gp63+46+22kDa, gp63+13.5+25+42kDa, gp63+46+42kDa, gp63+66kDa, and gp63+97kDa; 57.14% of protection was demonstrated with gp63+46+97+13.5kDa, gp63+46+97kDa, gp63+46+33kDa, and 71.43% protection for gp63 plus all proteins. The vaccine of gp63+46+40kDa that did not protect the mice, despite the good specific stimulation of lymphocytes (LSI = 7.60) and 10.77UI/ml of IFN-<FONT FACE="Symbol">g</font> production. When crude extract of L. (L.) amazonensis was used with BCG a 57.14% of protection was found after the first challenge and 28.57% after the second, the same result was observed for gp63. The data obtained with the vaccines can suggest that the future vaccine probably have to contain, except the 40kDa, a cocktail of proteins that would protect mice against cutaneous leishmaniasis.

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