Modulation of the anti-phosphorylcholine immune response duringTrichinella spiralisinfections in mice

Parasitology ◽  
1987 ◽  
Vol 95 (3) ◽  
pp. 583-592 ◽  
Author(s):  
F. M. Ubeira ◽  
J. Leiro ◽  
M. T. Santamarina ◽  
M. L. Sanmartin-Duran
Keyword(s):  
Immune Response ◽  
Life Cycle ◽  
Antibody Response ◽  
Red Blood Cells ◽  
Post Infection ◽  
Blood Cells ◽  
Trichinella Spiralis ◽  
Heterologous Antigen ◽  
Specific Suppression ◽  
Antigenic Fraction

SUMMARYThe nematodeTrichinella spiralisis able to modulate the antibody response, as measured by the plaque-forming cell (PFC) technique, to three thymus-dependent (TD) antigens: (1) a heterologous antigen unrelated to the parasite (sheep red blood cells (SRBC)); (2) an antigenic fraction, rich in phosphorylcholine (PC), obtained fromT. spiralis(FCpl) and (3) a heterologous antigen unrelated to the parasite, but sharing the PC epitope with the FCpl fraction (PC-KLH). During the life-cycle of the parasite in BCF1 mice, two opposing immunomodulating activities occur: (1) an immuno-potentiating activity in mice infected during the intestinal and larval migratory stages, for all three antigens, and (2) a carrier-specific immunosuppressive response in mice infected and immunized with the FCpl fraction during the muscle phase of the life-cycle. The anti-PC PFC response of these mice is dependent on the infection dose and decreases from day 35 post-infection (p.i.) until at least day 85 p.i.. The factor responsible for the stimulating effect observed during this stage is the presence of migratory larvae in the host. All the foregoing seems to indicate thatT. spiraliscan use specific suppression mechanisms to aid in its own survival.

scholarly journals Inside Scoop on Outside Proteins

2013 ◽  
Vol 82 (3) ◽  
pp. 921-923
Author(s):  
Jeffrey D. Dvorin
Keyword(s):  
Immune Response ◽  
Plasmodium Falciparum ◽  
Life Cycle ◽  
Red Blood Cells ◽  
Blood Cells ◽  
Current Issue ◽  
Detailed Examination ◽  
Content Type ◽  
Human Malaria ◽  
Essential Step

ABSTRACTInvasion into red blood cells is an essential step in the life cycle of parasites that cause human malaria. Antibodies targeting the key parasite proteins in this process are important for developing a protective immune response. In the current issue, Boyle and colleagues provide a detailed examination ofPlasmodium falciparuminvasion and specifically illuminate the fate of surface-exposed parasite proteins during and immediately after invasion.

scholarly journals Investigation of the immune status of mice during and following selective decontamination of the digestive tract

1989 ◽  
Vol 103 (2) ◽  
pp. 323-332 ◽  
Author(s):  
A. B. J. Speekenbrink ◽  
S. R. Alcock ◽  
D. M. V. Parrott
Keyword(s):  
Immune Response ◽  
Antibody Response ◽  
Red Blood Cells ◽  
Digestive Tract ◽  
Blood Cells ◽  
Cellular Response ◽  
Intensive Therapy ◽  
Selective Decontamination ◽  
Protein Antigens ◽  
Sheep Red Blood Cells

SUMMARYSelective decontamination of the digestive tract (SDD) employs oral antibiotics to eliminate aerobic Gram-negative bacilli while retaining the anaerobic flora. A combination of SDD and parenteral cefotaxime has recently been reported to strikingly reduce the incidence of infection in patients treated in an intensive therapy unit. The present study describes the effects of SDB and of cefotaxime on the immune response of mice to protein antigens. The in vivo cellular response to ovalbumin and sheep red blood cells was unchanged. However, SDD appeared to decrease the in vitro mitogenic response of spleen cells to phytohaemagglutinin, and cefotaxime similarly affected the response to Concanavalin A. The antibody response to sheep red blood cells was increased in the period after discontinuation of SDD. The antibody response was otherwise not affected. These results indicate that SDD is unlikely to have adverse effects on the immune response to protein antigens.

scholarly journals CELLS INVOLVED IN THE IMMUNE RESPONSE

1969 ◽  
Vol 129 (4) ◽  
pp. 757-774 ◽  
Author(s):  
Nabih I. Abdou ◽  
Maxwell Richter
Keyword(s):  
Bone Marrow ◽  
Immune Response ◽  
Red Blood Cells ◽  
Blood Cells ◽  
Bone Marrow Cells ◽  
Allogeneic Bone Marrow ◽  
Red Cells ◽  
Allogeneic Bone ◽  
Sheep Red Blood Cells ◽  
Sheep Red Cells

Irradiated rabbits given allogeneic bone marrow cells from normal adult donors responded to an injection of sheep red blood cells by forming circulating antibodies. Their spleen cells were also capable of forming many plaques using the hemolysis in gel technique, and were also capable of undergoing blastogenesis and mitosis and of incorporating tritiated thymidine upon exposure to the specific antigen in vitro. However, irradiated rabbits injected with allogeneic bone marrow obtained from rabbits injected with sheep red blood cells 24 hr prior to sacrifice (primed donors) were incapable of mounting an immune response after stimulation with sheep red cells. This loss of reactivity by the bone marrow from primed donors is specific for the antigen injected, since the immune response of the irradiated recipients to a non-cross-reacting antigen, the horse red blood cell, is unimpaired. Treatment of the bone marrow donors with high-titered specific antiserum to sheep red cells for 24 hr prior to sacrifice did not result in any diminished ability of their bone marrow cells to transfer antibody-forming capacity to sheep red blood cells. The significance of these results, with respect to the origin of the antigen-reactive and antibody-forming cells in the rabbit, is discussed.

THE LIFE CYCLE OF TRICHINELLA SPIRALIS: I. THE INTESTINAL PHASE OF DEVELOPMENT

1967 ◽  
Vol 45 (6) ◽  
pp. 1255-1260 ◽  
Author(s):  
C. S. Shanta ◽  
E. Meerovitch
Keyword(s):  
Life Cycle ◽  
Post Infection ◽  
Sexual Maturity ◽  
Trichinella Spiralis ◽  
Seminal Vesicles ◽  
Intestinal Phase ◽  
Experimental Infections

In experimental infections in mice, Trichinella spiralis larvae in the intestines molted twice before reaching sexual maturity. In both sexes, the first molt occurred between 12 and 16 hours post infection; in males, the second molt occurred between 24 and 32 hours, and in females, between 22 and 30 hours. The females were inseminated after the 36th hour post infection, but some males had spermatozoa in the seminal vesicles before the completion of the second molt. Structures, believed to be amphids, were observed after 2 hours post infection; they increased in size up to the 6th hour, after which they regressed and finally disappeared. The function of these amphids is believed to be related to osmoregulation.

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