Tumor necrosis factor-alpha (TNF-alpha) is critically involved in the pathogenesis of several chronic inflammatory diseases. Monoclonal antibodies against TNF-alpha are currently used for the treatment of rheumatoid arthritis and Crohn's disease. This report describes a simple and effective method for active immunization against self TNF-alpha. This vaccination approach leads to a T-cell-dependent polyclonal and sustainable anti-TNF-alpha autoantibody response that declines upon discontinuation of booster injections. The autoantibodies are elicited by injecting modified recombinant TNF-alpha molecules containing foreign immunodominant T-helper epitopes. In mice immunized with such molecules, the symptoms of experimental cachexia and type II collagen-induced arthritis are ameliorated. These results suggest that vaccination against TNF-alpha may be a useful approach for the treatment of rheumatoid arthritis and other chronic inflammatory diseases.
Tremendous progress has been made over the last ten years on East Coast fever (ECF) research. Publication of a reference genome sequence of Theileria parva, the causative agent of ECF, has led to a more thorough characterization of the genotypic and antigenic diversity of the pathogen. It also facilitated identification of antigens that are targets of bovine major histocompatibility complex class I restricted cytotoxic T-lymphocytes (CTLs), induced by a live parasite-based infection and treatment method (ITM) vaccine. This has led to improved knowledge of epitope-specific T-cell responses to ITM that most likely contribute to the phenomenon of strain-specific immunity. The Muguga cocktail ITM vaccine, which provides broad-spectrum immunity to ECF is now a registered product in three countries in eastern Africa. Effort is directed at improving and scaling up the production process to make this vaccine more widely available on a commercial basis in the region. Meanwhile, research to develop a subunit vaccine based on parasite neutralizing antibodies and CTLs has been revived through convening of a research consortium to develop proof-of-concept for a next generation vaccine. Many new scientific and technical advances are facilitating this objective. Hence, the next decade promises even more progress toward an improved control of ECF.
Peptide-major histocompatibility complex (p-MHC) class I tetramer complexes have facilitated the early detection and functional characterisation of epitope specific CD8+ cytotoxic T lymphocytes (CTL). Here, we report on the generation of seven recombinant bovine leukocyte antigens (BoLA) and recombinant bovine β2-microglobulin from which p-MHC class I tetramers can be derived in ~48 h. We validated a set of p-MHC class I tetramers against a panel of CTL lines specific to seven epitopes on five different antigens of Theileria parva, a protozoan pathogen causing the lethal bovine disease East Coast fever. One of the p-MHC class I tetramers was tested in ex vivo assays and we detected T. parva specific CTL in peripheral blood of cattle at day 15-17 post-immunization with a live parasite vaccine. The algorithm NetMHCpan predicted alternative epitope sequences for some of the T. parva CTL epitopes. Using an ELISA assay to measure peptide-BoLA monomer formation and p-MHC class I tetramers of new specificity, we demonstrate that a predicted alternative epitope Tp229-37 rather than the previously reported Tp227-37 epitope is the correct Tp2 epitope presented by BoLA-6*04101. We also verified the prediction by NetMHCpan that the Tp587-95 epitope reported as BoLA-T5 restricted can also be presented by BoLA-1*02301, a molecule similar in sequence to BoLA-T5. In addition, Tp587-95 specific bovine CTL were simultaneously stained by Tp5-BoLA-1*02301 and Tp5-BoLA-T5 tetramers suggesting that one T cell receptor can bind to two different BoLA MHC class I molecules presenting the Tp587-95 epitope and that these BoLA molecules fall into a single functional supertype.
Rapid diagnosis based on naked-eye colorimetric detection remains challenging, but it
could build new capacities for molecular point-of-care testing (POCT). In this study, we
evaluated the performance of 16 types of single-stranded DNA-fluorophore-quencher
(ssDNA-FQ) reporters for use with clusters of regularly spaced short palindrome repeats
(CRISPR)/Cas12a-based visual colorimetric assays. Among them, nine ssDNA-FQ reporters
were found to be suitable for direct visual colorimetric detection, with especially very
strong performance using ROX-labeled reporters. We optimized the reaction concentrations
of these ssDNA-FQ reporters for a naked-eye read-out of assay results (no transducing
component required for visualization). In particular, we developed a convolutional
neural network algorithm to standardize and automate the analytical colorimetric
assessment of images and integrated this into the MagicEye mobile phone software. A
field-deployable assay platform named RApid VIsual CRISPR (RAVI-CRISPR) based on a
ROX-labeled reporter with isothermal amplification and CRISPR/Cas12a targeting was
established. We deployed RAVI-CRISPR in a single tube toward an instrument-less
colorimetric POCT format that required only a portable rechargeable hand warmer for
incubation. The RAVI-CRISPR was successfully used for the high-sensitivity detection of
severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) and African swine fever
virus (ASFV). Our study demonstrates this RAVI-CRISPR/MagicEye system to be suitable for
distinguishing different pathogenic nucleic acid targets with high specificity and
sensitivity as the simplest-to-date platform for rapid pen- or bed-side testing.
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