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Influence of Brucella Endotoxins on the Initiation of Antibody-Forming Spleen Cells in Mice Immunized with Sheep Red Blood Cells
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Changes in the formation of antibodies to sheep red blood cells (sRBC) in the presence of
Brucella
extracts was studied in mice whose spleen cells were assayed by the Jerne procedure. Two strains of female mice were employed.
Brucella
extracts were prepared: (i) by trichloroacetic acid extraction (LPSN), (ii) by phenol extraction (LPS), and (iii) by hot acetic acid hydrolysis (Ps).
B. abortus
LPSN and
B. melitensis
LPSN or LPS, administered with sRBC, stimulated the specific response to sRBC, but only at high doses of endotoxins.
B. abortus
LPSN and
B. melitensis
LPSN suppressed nonspecific responses against horse red blood cells (hRBC), in contrast to the typical events following administration of
Serratia marcescens
endotoxin (or endotoxins from other ubiquitous organisms). In CD-1 mice,
B. abortus
Ps depressed the specific anti-sRBC response. Attempts to presensitize mice with
abortus
LPSN resulted in a stimulation of the response to sRBC, but pretreatment with
B. melitensis
LPSN had an inhibitory effect. When injected alone,
Brucella
endotoxins activated anti-sRBC antibody-forming cells but not anti-hRBC cells.
B. abortus
Ps was unable to modify the background number of anti-sRBC cells and inhibited the hRBC response. These data suggest (i) that there exists a “common antigen” between
Brucella
cells and sRBC and (ii) that the so-called primary response to endotoxins from ubiquitous organisms represents a secondary response to already naturally sensitized animals.
American Society for Microbiology
Title: Influence of
Brucella
Endotoxins on the Initiation of Antibody-Forming Spleen Cells in Mice Immunized with Sheep Red Blood Cells
Description:
Changes in the formation of antibodies to sheep red blood cells (sRBC) in the presence of
Brucella
extracts was studied in mice whose spleen cells were assayed by the Jerne procedure.
Two strains of female mice were employed.
Brucella
extracts were prepared: (i) by trichloroacetic acid extraction (LPSN), (ii) by phenol extraction (LPS), and (iii) by hot acetic acid hydrolysis (Ps).
B.
abortus
LPSN and
B.
melitensis
LPSN or LPS, administered with sRBC, stimulated the specific response to sRBC, but only at high doses of endotoxins.
B.
abortus
LPSN and
B.
melitensis
LPSN suppressed nonspecific responses against horse red blood cells (hRBC), in contrast to the typical events following administration of
Serratia marcescens
endotoxin (or endotoxins from other ubiquitous organisms).
In CD-1 mice,
B.
abortus
Ps depressed the specific anti-sRBC response.
Attempts to presensitize mice with
abortus
LPSN resulted in a stimulation of the response to sRBC, but pretreatment with
B.
melitensis
LPSN had an inhibitory effect.
When injected alone,
Brucella
endotoxins activated anti-sRBC antibody-forming cells but not anti-hRBC cells.
B.
abortus
Ps was unable to modify the background number of anti-sRBC cells and inhibited the hRBC response.
These data suggest (i) that there exists a “common antigen” between
Brucella
cells and sRBC and (ii) that the so-called primary response to endotoxins from ubiquitous organisms represents a secondary response to already naturally sensitized animals.
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