Litomosoides sigmodontis: Vaccine-induced immune responses against Wolbachia surface protein can enhance the survival of filarial nematodes during primary infection

2008 ◽  
Vol 118 (2) ◽  
pp. 285-289 ◽  
Author(s):  
Tracey J. Lamb ◽  
Anjanette Harris ◽  
Laetitia Le Goff ◽  
Andrew F. Read ◽  
Judith E. Allen
Keyword(s):  
Immune Responses ◽  
Primary Infection ◽  
Surface Protein ◽  
Wolbachia Surface Protein ◽  
Litomosoides Sigmodontis ◽  
Filarial Nematodes

scholarly journals The Major Surface Protein ofWolbachiaEndosymbionts in Filarial Nematodes Elicits Immune Responses through TLR2 and TLR4

2004 ◽  
Vol 173 (1) ◽  
pp. 437-445 ◽  
Author(s):  
Norbert W. Brattig ◽  
Chiara Bazzocchi ◽  
Carsten J. Kirschning ◽  
Norbert Reiling ◽  
Dietrich W. Büttner ◽  
...  
Keyword(s):  
Immune Responses ◽  
Surface Protein ◽  
Major Surface Protein ◽  
Filarial Nematodes ◽  
Major Surface

scholarly journals Wolbachia surface protein induces innate immune responses in mosquito cells

2012 ◽  
Vol 12 (Suppl 1) ◽  
pp. S11 ◽  
Author(s):  
Sofia B Pinto ◽  
Mara Mariconti ◽  
Chiara Bazzocchi ◽  
Claudio Bandi ◽  
Steven P Sinkins
Keyword(s):  
Immune Responses ◽  
Surface Protein ◽  
Innate Immune ◽  
Innate Immune Responses ◽  
Wolbachia Surface Protein ◽  
Mosquito Cells

scholarly journals Immunoglobulin G Antibodies against the Endosymbionts of Filarial Nematodes (Wolbachia) in Patients with Pulmonary Dirofilariasis

2003 ◽  
Vol 10 (1) ◽  
pp. 180-181 ◽  
Author(s):  
F. Simón ◽  
G. Prieto ◽  
R. Morchón ◽  
C. Bazzocchi ◽  
C. Bandi ◽  
...  
Keyword(s):  
Immunoglobulin G ◽  
Dirofilaria Immitis ◽  
Surface Protein ◽  
Igg Antibodies ◽  
Healthy Individuals ◽  
Bacterial Endosymbiont ◽  
Filarial Nematodes ◽  
Pulmonary Dirofilariasis ◽  
Diagnostic Applications

ABSTRACT The dog parasite Dirofilaria immitis can infect humans. Patients with pulmonary dirofilariasis were tested for immunoglobulin G (IgG) antibodies against the surface protein of Wolbachia, the bacterial endosymbiont of D. immitis. These patients showed significantly higher IgG titers than healthy individuals from areas in which D. immitis was endemic as well as areas in which it was not endemic. Titration of anti-Wolbachia surface protein IgG could become useful for diagnostic applications.

scholarly journals Robust SARS-CoV-2-specific T-cell immunity is maintained at 6 months following primary infection

2020 ◽  
Author(s):  
Jianmin Zuo ◽  
Alex Dowell ◽  
Hayden Pearce ◽  
Kriti Verma ◽  
Heather Long ◽  
...  
Keyword(s):  
Immune Response ◽  
T Cell ◽  
Immune Responses ◽  
Antibody Level ◽  
Primary Infection ◽  
Natural Infection ◽  
T Cell Responses ◽  
Symptomatic Infection ◽  
Cell Responses ◽  
Cell Immunity

Abstract The immune response to SARS-CoV-2 is critical in both controlling primary infection and preventing re-infection. However, there is concern that immune responses following natural infection may not be sustained and that this may predispose to recurrent infection. We analysed the magnitude and phenotype of the SARS-CoV-2 cellular immune response in 100 donors at six months following primary infection and related this to the profile of antibody level against spike, nucleoprotein and RBD over the previous six months. T-cell immune responses to SARS-CoV-2 were present by ELISPOT or ICS analysis in all donors and are characterised by predominant CD4+ T cell responses with strong IL-2 cytokine expression. Median T-cell responses were 50% higher in donors who had experienced an initial symptomatic infection indicating that the severity of primary infection establishes a ‘setpoint’ for cellular immunity that lasts for at least 6 months. The T-cell responses to both spike and nucleoprotein/membrane proteins were strongly correlated with the peak antibody level against each protein. The rate of decline in antibody level varied between individuals and higher levels of nucleoprotein-specific T cells were associated with preservation of NP-specific antibody level although no such correlation was observed in relation to spike-specific responses. In conclusion, our data are reassuring that functional SARS-CoV-2-specific T-cell responses are retained at six months following infection although the magnitude of this response is related to the clinical features of primary infection.

scholarly journals Genetic diversity and immunogenicity of the merozoite surface protein 1 C-terminal 19-kDa fragment of Plasmodium ovale imported from Africa into China

2021 ◽  
Vol 14 (1) ◽  
Author(s):  
Qinwen Xu ◽  
Sihong Liu ◽  
Kokouvi Kassegne ◽  
Bo Yang ◽  
Jiachen Lu ◽  
...  
Keyword(s):  
Genetic Diversity ◽  
Immune Responses ◽  
Expression System ◽  
Surface Protein ◽  
Merozoite Surface Protein ◽  
Enzyme Linked Immunosorbent Assay ◽  
High Avidity ◽  
Plasmodium Ovale ◽  
Merozoite Surface Protein 1 ◽  
Proliferation Assays

Abstract Background Merozoite surface protein 1 (MSP1) plays an essential role in erythrocyte invasion by malaria parasites. The C-terminal 19-kDa region of MSP1 has long been considered one of the major candidate antigens for a malaria blood-stage vaccine against Plasmodium falciparum. However, there is limited information on the C-terminal 19-kDa region of Plasmodium ovale MSP1 (PoMSP119). This study aims to analyze the genetic diversity and immunogenicity of PoMSP119. Methods A total of 37 clinical Plasmodium ovale isolates including Plasmodium ovale curtisi and Plasmodium ovale wallikeri imported from Africa into China and collected during the period 2012–2016 were used. Genomic DNA was used to amplify P. ovale curtisi (poc) msp119 (pocmsp119) and P. ovale wallikeri (pow) msp119 (powmsp119) genes by polymerase chain reaction. The genetic diversity of pomsp119 was analyzed using the GeneDoc version 6 programs. Recombinant PoMSP119 (rPoMSP119)-glutathione S-transferase (GST) proteins were expressed in an Escherichia coli expression system and analyzed by western blot. Immune responses in BALB/c mice immunized with rPoMSP119-GST were determined using enzyme-linked immunosorbent assay. In addition, antigen-specific T cell responses were assessed by lymphocyte proliferation assays. A total of 49 serum samples from healthy individuals and individuals infected with P. ovale were used for the evaluation of natural immune responses by using protein microarrays. Results Sequences of pomsp119 were found to be thoroughly conserved in all the clinical isolates. rPoMSP119 proteins were efficiently expressed and purified as ~ 37-kDa proteins. High antibody responses in mice immunized with rPoMSP119-GST were observed. rPoMSP119-GST induced high avidity indexes, with an average of 92.57% and 85.32% for rPocMSP119 and rPowMSP119, respectively. Cross-reactivity between rPocMSP119 and rPowMSP119 was observed. Cellular immune responses to rPocMSP119 (69.51%) and rPowMSP119 (52.17%) induced in rPocMSP119- and rPowMSP119-immunized mice were found in the splenocyte proliferation assays. The sensitivity and specificity of rPoMSP119-GST proteins for the detection of natural immune responses in patients infected with P. ovale were 89.96% and 75%, respectively. Conclusions This study revealed highly conserved gene sequences of pomsp119. In addition, naturally acquired humoral immune responses against rPoMSP1 were observed in P. ovale infections, and high immunogenicity of rPoMSP119 in mice was also identified. These instructive findings should encourage further testing of PoMSP119 for rational vaccine design. Graphical abstract

Experimental Otitis Media in Chinchillas

1980 ◽  
Vol 89 (3_suppl) ◽  
pp. 344-350 ◽  
Author(s):  
Daniel M. Lewis ◽  
Samuel J. Meadema ◽  
James L. Schram ◽  
David J. Lim
Keyword(s):  
Immune System ◽  
Immune Responses ◽  
Otitis Media ◽  
Middle Ear ◽  
Primary Infection ◽  
Intramuscular Injection ◽  
Bacterial Suspension ◽  
Immune Mechanisms ◽  
Development Of Resistance ◽  
Type 3

Otitis media was induced in chinchillas by intrabullar injection of type 3 Streptococcus pneumoniae. It was found that the severity of a primary infection was related to the dose of bacteria injected, and animals that had recovered from a primary infection were resistant to reinfection with type 3 S pneumoniae. Middle ear effusions from infected animals contained antibodies to type 3 pneumococcal polysaccharide, whereas the sera of these animals lacked this antibody, suggesting that resistance to reinfection was due to local immune mechanisms. This idea was tested by immunizing chinchillas by various routes. Animals immunized with formalin-killed type 3 S pneumoniae by intramuscular injection (to stimulate the systemic immune system) or by intranasal inoculation (to stimulate the secretory immune system) were found to be susceptible to infection with type 3 pneumococcus, while animals immunized by inoculation of bacterial suspension directly into the middle ear were resistant to infection. In addition, we found that ampicillin treatment of a primary infection blocks the development of resistance since antibiotic-treated animals were susceptible to reinfection with the type 3 pneumococcus. These results indicate that chinchillas develop an immunity to pneumococcal otitis media following recovery from primary infection and that this immunity is mediated primarily by local immune mechanisms rather than systemic immune responses.

Sign in / Sign up

Export Citation Format

Share Document