RÉSUMÉ
Current prophylactic human immunodeficiency virus 1 (HIV-1) vaccine research aims to elicit broadly neutralizing antibodies (bnAbs). Membrane-proximal external region (MPER)-targeting bnAbs, such as 10E8, provide exceptionally broad neutralization, but some are autoreactive. Here, we generated humanized B cell antigen receptor knock-in mouse models to test whether a series of germline-targeting immunogens could drive MPER-specific precursors toward bnAbs. We found that recruitment of 10E8 precursors to germinal centers (GCs) required a minimum affinity for germline-targeting immunogens, but the GC residency of MPER precursors was brief due to displacement by higher-affinity endogenous B cell competitors. Higher-affinity germline-targeting immunogens extended the GC residency of MPER precursors, but robust long-term GC residency and maturation were only observed for MPER-HuGL18, an MPER precursor clonotype able to close the affinity gap with endogenous B cell competitors in the GC. Thus, germline-targeting immunogens could induce MPER-targeting antibodies, and B cell residency in the GC may be regulated by a precursor-competitor affinity gap.
Sujet(s)
Affinité des anticorps , Lymphocytes B , Centre germinatif , Anticorps anti-VIH , VIH-1 (Virus de l'Immunodéficience Humaine de type 1) , Centre germinatif/immunologie , Animaux , Souris , Humains , Lymphocytes B/immunologie , VIH-1 (Virus de l'Immunodéficience Humaine de type 1)/immunologie , Anticorps anti-VIH/immunologie , Affinité des anticorps/immunologie , Anticorps neutralisants/immunologie , Infections à VIH/immunologie , Vaccins contre le SIDA/immunologie , Récepteurs pour l'antigène des lymphocytes B/métabolisme , Récepteurs pour l'antigène des lymphocytes B/immunologie , Techniques de knock-in de gènes , Souris transgéniques , Anticorps neutralisants à large spectre/immunologie , Souris de lignée C57BLRÉSUMÉ
Eliciting broadly neutralizing antibodies (bnAbs) is the core of HIV vaccine design. bnAbs specific to the V2-apex region of the HIV envelope acquire breadth and potency with modest somatic hypermutation, making them attractive vaccination targets. To evaluate Apex germline-targeting (ApexGT) vaccine candidates, we engineered knockin (KI) mouse models expressing the germline B cell receptor (BCR) of the bnAb PCT64. We found that high affinity of the ApexGT immunogen for PCT64-germline BCRs was necessary to specifically activate KI B cells at human physiological frequencies, recruit them to germinal centers, and select for mature bnAb mutations. Relative to protein, mRNA-encoded membrane-bound ApexGT immunization significantly increased activation and recruitment of PCT64 precursors to germinal centers and lowered their affinity threshold. We have thus developed additional models for HIV vaccine research, validated ApexGT immunogens for priming V2-apex bnAb precursors, and identified mRNA-LNP as a suitable approach to substantially improve the B cell response.
Sujet(s)
Vaccins contre le SIDA , Infections à VIH , VIH-1 (Virus de l'Immunodéficience Humaine de type 1) , Souris , Humains , Animaux , Anticorps anti-VIH , Anticorps neutralisants à large spectre , Anticorps neutralisants , ARN messager/génétique , Produits du gène env du virus de l'immunodéficience humaineRÉSUMÉ
Repeat antigens, such as the Plasmodium falciparum circumsporozoite protein (PfCSP), use both sequence degeneracy and structural diversity to evade the immune response. A few PfCSP-directed antibodies have been identified that are effective at preventing malaria infection, including CIS43, but how these repeat-targeting antibodies might be improved has been unclear. Here, we engineered a humanized mouse model in which B cells expressed inferred human germline CIS43 (iGL-CIS43) B cell receptors and used both vaccination and bioinformatic analysis to obtain variant CIS43 antibodies with improved protective capacity. One such antibody, iGL-CIS43.D3, was significantly more potent than the current best-in-class PfCSP-directed antibody. We found that vaccination with a junctional epitope peptide was more effective than full-length PfCSP at recruiting iGL-CIS43 B cells to germinal centers. Structure-function analysis revealed multiple somatic hypermutations that combinatorically improved protection. This mouse model can thus be used to understand vaccine immunogens and to develop highly potent anti-malarial antibodies.
Sujet(s)
Sous-populations de lymphocytes B/immunologie , Épitopes/immunologie , Vaccins contre le paludisme/immunologie , Paludisme/immunologie , Plasmodium falciparum/physiologie , Protéines de protozoaire/immunologie , Vaccins à ADN/immunologie , Transfert adoptif , Animaux , Anticorps antiprotozoaires/métabolisme , Modèles animaux de maladie humaine , Épitopes/génétique , Génie génétique , Humains , Échappement immunitaire , Immunogénicité des vaccins , Souris , Souris SCID , Protéines de protozoaire/génétique , Relation structure-activité , VaccinationRÉSUMÉ
B-cell receptor (BCR) knock-in (KI) mouse models play an important role in vaccine development and fundamental immunological studies. However, the time required to generate them poses a bottleneck. Here we report a one-step CRISPR/Cas9 KI methodology to combine the insertion of human germline immunoglobulin heavy and light chains at their endogenous loci in mice. We validate this technology with the rapid generation of three BCR KI lines expressing native human precursors, instead of computationally inferred germline sequences, to HIV broadly neutralizing antibodies. We demonstrate that B cells from these mice are fully functional: upon transfer to congenic, wild type mice at controlled frequencies, such B cells can be primed by eOD-GT8 60mer, a germline-targeting immunogen currently in clinical trials, recruited to germinal centers, secrete class-switched antibodies, undergo somatic hypermutation, and differentiate into memory B cells. KI mice expressing functional human BCRs promise to accelerate the development of vaccines for HIV and other infectious diseases.
Sujet(s)
Lymphocytes B/métabolisme , Systèmes CRISPR-Cas/génétique , Récepteurs pour l'antigène des lymphocytes B/métabolisme , Animaux , Lymphocytes B/immunologie , Anticorps neutralisants à large spectre/immunologie , Systèmes CRISPR-Cas/immunologie , Lignée cellulaire , Techniques de knock-in de gènes/méthodes , Centre germinatif/immunologie , Centre germinatif/métabolisme , Cellules HEK293 , VIH-1 (Virus de l'Immunodéficience Humaine de type 1)/immunologie , Humains , Mâle , Souris , Souris de lignée C57BL , Modèles animaux , Récepteurs pour l'antigène des lymphocytes B/immunologieRÉSUMÉ
Vaccine induction of broadly neutralizing antibodies (bnAbs) to HIV remains a major challenge. Germline-targeting immunogens hold promise for initiating the induction of certain bnAb classes; yet for most bnAbs, a strong dependence on antibody heavy chain complementarity-determining region 3 (HCDR3) is a major barrier. Exploiting ultradeep human antibody sequencing data, we identified a diverse set of potential antibody precursors for a bnAb with dominant HCDR3 contacts. We then developed HIV envelope trimer-based immunogens that primed responses from rare bnAb-precursor B cells in a mouse model and bound a range of potential bnAb-precursor human naïve B cells in ex vivo screens. Our repertoire-guided germline-targeting approach provides a framework for priming the induction of many HIV bnAbs and could be applied to most HCDR3-dominant antibodies from other pathogens.
Sujet(s)
Vaccins contre le SIDA/génétique , Vaccins contre le SIDA/immunologie , Anticorps neutralisants à large spectre/immunologie , Évolution moléculaire dirigée/méthodes , Anticorps anti-VIH/immunologie , Immunogénicité des vaccins , Produits du gène env du virus de l'immunodéficience humaine/génétique , Produits du gène env du virus de l'immunodéficience humaine/immunologie , Transfert adoptif , Séquence d'acides aminés , Animaux , Lymphocytes B/immunologie , Anticorps neutralisants à large spectre/composition chimique , Régions déterminant la complémentarité/immunologie , Modèles animaux de maladie humaine , Cellules HEK293 , Anticorps anti-VIH/composition chimique , Humains , Souris , Souris knockout , Précurseurs lymphoïdes B/immunologieRÉSUMÉ
Here, we describe a one-step, in vivo CRISPR/Cas9 nuclease-mediated strategy to generate knock-in mice. We produced knock-in (KI) mice wherein a 1.9-kb DNA fragment bearing a pre-arranged human B-cell receptor heavy chain was recombined into the native murine immunoglobulin locus. Our methodology relies on Cas9 nuclease-induced double-stranded breaks directed by two sgRNAs to occur within the specific target locus of fertilized oocytes. These double-stranded breaks are subsequently repaired via homology-directed repair by a plasmid-borne template containing the pre-arranged human immunoglobulin heavy chain. To validate our knock-in mouse model, we examined the expression of the KI immunoglobulin heavy chains by following B-cell development and performing single B-cell receptor sequencing. We optimized this strategy to generate immunoglobulin KI mice in a short amount of time with a high frequency of homologous recombination (30-50%). In the future, we envision that such knock-in mice will provide much needed vaccination models to evaluate immunoresponses against immunogens specific for various infectious diseases.
Sujet(s)
Lymphocytes B/immunologie , Systèmes CRISPR-Cas , Techniques de knock-in de gènes/méthodes , Chaines lourdes des immunoglobulines , Animaux , Lymphocytes B/cytologie , Humains , Chaines lourdes des immunoglobulines/génétique , Chaines lourdes des immunoglobulines/immunologie , Souris , Souris transgéniquesRÉSUMÉ
Arboviruses can cause a variety of clinical signs, including febrile illness, arthritis, encephalitis, and hemorrhagic fever. The recent Zika epidemic highlighted the possibility that arboviruses may also negatively affect the male reproductive tract. In this study, we focused on bluetongue virus (BTV), the causative agent of bluetongue and one of the major arboviruses of ruminants. We show that rams that recovered from bluetongue displayed signs of testicular degeneration and azoospermia up to 100 days after the initial infection. Importantly, testicular degeneration was induced in rams experimentally infected with either a high (BTV-1IT2006)- or a low (BTV-1IT2013)-virulence strain of BTV. Rams infected with the low-virulence BTV strain displayed testicular lesions in the absence of other major clinical signs. Testicular lesions in BTV-infected rams were due to viral replication in the endothelial cells of the peritubular areas of the testes, resulting in stimulation of a type I interferon response, reduction of testosterone biosynthesis by Leydig cells and destruction of Sertoli cells and the blood-testis barrier in more severe cases. Hence, BTV induces testicular degeneration and disruption of spermatogenesis by replicating solely in the endothelial cells of the peritubular areas unlike other gonadotropic viruses. This study shows that a naturally occurring arboviral disease can cause testicular degeneration and affect male fertility at least temporarily.IMPORTANCE During the recent Zika epidemic, it has become apparent that arboviruses could potentially cause reproductive health problems in male patients. Little is known regarding the effects that arboviruses have on the male reproductive tract. Here, we studied bluetongue virus (BTV), an arbovirus of ruminants, and its effects on the testes of rams. We show that BTV was able to induce testicular degeneration in naturally and experimentally infected rams. Testicular degeneration was caused by BTV replication in the endothelial cells of the peritubular area surrounding the seminiferous tubules (the functional unit of the testes) and was associated with a localized type I interferon response, destruction of the cells supporting the developing germinal cells (Sertoli cells), and reduction of testosterone synthesis. As a result of BTV infection, rams became azoospermic. This study highlights that problems in the male reproductive tract caused by arboviruses could be more common than previously thought.
Sujet(s)
Virus de la langue bleue/pathogénicité , Fièvre catarrhale du mouton/complications , Endothélium vasculaire/anatomopathologie , Infertilité masculine/étiologie , Maladies des ovins/étiologie , Spermatogenèse , Testicule/anatomopathologie , Animaux , Fièvre catarrhale du mouton/anatomopathologie , Fièvre catarrhale du mouton/virologie , Endothélium vasculaire/métabolisme , Endothélium vasculaire/virologie , Infertilité masculine/anatomopathologie , Mâle , Ovis , Maladies des ovins/anatomopathologie , Testicule/métabolisme , Testicule/virologie , Testostérone/analyse , Virulence , Réplication viraleRÉSUMÉ
Sheep are not only a major livestock species globally, they are also an important large animal model for biomedical research and have contributed to our understanding of the ontogeny and architecture of the mammalian immune system. In this study, we applied immunohistochemistry and multicolor immunofluorescence in fixed and paraffin-embedded lymph nodes to phenotype the key populations of antigen presenting cells, lymphocytes, and stromal cells that orchestrate the host adaptive immune response. We used an extensive panel of antibodies directed against markers associated with dendritic cells (MHC class II, CD83, and CD208), macrophages (CD11b, CD163, and CD169), stromal cells (CNA.42, S100, and CD83), and lymphocytes (CD3, Pax5, CD4, CD8). Using different methods of tissue fixation and antigen retrieval, we provide a detailed immunophenotyping of sheep lymph nodes including the identification of potential subpopulations of antigen presenting cells and stromal cells. By characterizing cells expressing combinations of these markers in the context of their morphology and location within the lymph node architecture, we provide valuable new tools to investigate the structure, activation, and regulation of the sheep immune system in health and disease.
Sujet(s)
Cellules présentatrices d'antigène/immunologie , Immunophénotypage/méthodes , Noeuds lymphatiques/immunologie , Lymphocytes/immunologie , Inclusion en paraffine/méthodes , Cellules stromales/immunologie , Animaux , Cellules présentatrices d'antigène/métabolisme , Antigènes CD/immunologie , Antigènes CD/métabolisme , Cellules dendritiques/immunologie , Cellules dendritiques/métabolisme , Immunohistochimie , Noeuds lymphatiques/cytologie , Noeuds lymphatiques/métabolisme , Lymphocytes/métabolisme , Macrophages/immunologie , Macrophages/métabolisme , Ovis , Cellules stromales/métabolismeRÉSUMÉ
Arboviruses cause acute diseases that increasingly affect global health. We used bluetongue virus (BTV) and its natural sheep host to reveal a previously uncharacterized mechanism used by an arbovirus to manipulate host immunity. Our study shows that BTV, similarly to other antigens delivered through the skin, is transported rapidly via the lymph to the peripheral lymph nodes. Here, BTV infects and disrupts follicular dendritic cells, hindering B-cell division in germinal centers, which results in a delayed production of high affinity and virus neutralizing antibodies. Moreover, the humoral immune response to a second antigen is also hampered in BTV-infected animals. Thus, an arbovirus can evade the host antiviral response by inducing an acute immunosuppression. Although transient, this immunosuppression occurs at the critical early stages of infection when a delayed host humoral immune response likely affects virus systemic dissemination and the clinical outcome of disease.
Sujet(s)
Maladies de l'animal/immunologie , Cellules dendritiques folliculaires/immunologie , Interactions hôte-pathogène/immunologie , Tolérance immunitaire , Maladies virales/médecine vétérinaire , Virus/immunologie , Maladies de l'animal/virologie , Animaux , Lymphocytes B/immunologie , Lymphocytes B/métabolisme , Fièvre catarrhale du mouton/immunologie , Fièvre catarrhale du mouton/virologie , Virus de la langue bleue/génétique , Virus de la langue bleue/immunologie , Cellules dendritiques folliculaires/métabolisme , Cellules endothéliales/virologie , Régulation de l'expression des gènes viraux , Immunohistochimie , Noeuds lymphatiques/immunologie , Macrophages/immunologie , Macrophages/virologie , Ovis , Cellules stromales , Virémie/immunologie , Virulence , Virus/génétiqueRÉSUMÉ
Viruses have often evolved overlapping reading frames in order to maximize their coding capacity. Until recently, the segmented dsRNA genome of viruses of the Orbivirus genus was thought to be monocistronic, but the identification of the bluetongue virus (BTV) NS4 protein changed this assumption. A small ORF in segment 10, overlapping the NS3 ORF in the +1 position, is maintained in more than 300 strains of the 27 different BTV serotypes and in more than 200 strains of the phylogenetically related African horse sickness virus (AHSV). In BTV, this ORF (named S10-ORF2 in this study) encodes a putative protein 50-59 residues in length and appears to be under strong positive selection. HA- or GFP-tagged versions of S10-ORF2 expressed from transfected plasmids localized within the nucleoli of transfected cells, unless a putative nucleolar localization signal was mutated. S10-ORF2 inhibited gene expression, but not RNA translation, in transient transfection reporter assays. In both mammalian and insect cells, BTV S10-ORF2 deletion mutants (BTV8ΔS10-ORF2) displayed similar replication kinetics to wt virus. In vivo, S10-ORF2 deletion mutants were pathogenic in mouse models of disease. Although further evidence is required for S10-ORF2 expression during infection, the data presented provide an initial characterization of this ORF.
Sujet(s)
Virus de la langue bleue/génétique , Fièvre catarrhale du mouton/virologie , Génome viral , Cadres ouverts de lecture , Protéines virales/génétique , Animaux , Virus de la langue bleue/classification , Virus de la langue bleue/métabolisme , Lignée cellulaire , Souris , Phylogenèse , Protéines virales/métabolismeRÉSUMÉ
Bovine neonatal pancytopenia (BNP) is a recently described haemorrhagic disease of calves characterised by thrombocytopenia, leucopenia and bone marrow depletion. Feeding colostrum from cows that have previously produced a BNP affected calf has been shown to induce the disease in some calves, leading to the hypothesis that alloantibodies in colostrum from dams of affected calves mediate destruction of blood and bone marrow cells in the recipient calves. The aims of the current experimental study were first to confirm the role of colostrum-derived antibody in mediating the disease and second to investigate the haematopoietic cell lineages and maturation stages depleted by the causative antibodies. Clinical, haematological and pathological changes were examined in 5 calves given a standardised pool of colostrum from known BNP dams, and 5 control calves given an equivalent pool of colostrum from non-BNP dams. All calves fed challenge colostrum showed progressive depletion of bone marrow haematopoietic cells and haematological changes consistent with the development of BNP. Administration of a standardised dose of the same colostrum pool to each calf resulted in a consistent response within the groups, allowing detailed interpretation of the cellular changes not previously described. Analyses of blood and serial bone marrow changes revealed evidence of differential effects on different blood cell lineages. Peripheral blood cell depletion was confined to leucocytes and platelets, while bone marrow damage occurred to the primitive precursors and lineage committed cells of the thrombocyte, lymphocyte and monocyte lineages, but only to the more primitive precursors in the neutrophil, erythrocyte and eosinophil lineages. Such differences between lineages may reflect cell type-dependent differences in levels of expression or conformational nature of the target antigens.
Sujet(s)
Maladies des bovins/immunologie , Colostrum/immunologie , Alloanticorps/administration et posologie , Alloanticorps/effets indésirables , Pancytopénie/médecine vétérinaire , Animaux , Animaux nouveau-nés , Cellules sanguines/immunologie , Cellules sanguines/anatomopathologie , Moelle osseuse/immunologie , Moelle osseuse/anatomopathologie , Bovins , Maladies des bovins/sang , Maladies des bovins/anatomopathologie , Lignage cellulaire/immunologie , Femelle , Gènes MHC de classe II , Cellules souches hématopoïétiques/immunologie , Cellules souches hématopoïétiques/anatomopathologie , Modèles immunologiques , Pancytopénie/immunologie , Pancytopénie/anatomopathologie , GrossesseRÉSUMÉ
BACKGROUND: Bovine neonatal pancytopenia (BNP) is a syndrome characterised by thrombocytopenia associated with marked bone marrow destruction in calves, widely reported since 2007 in several European countries and since 2011 in New Zealand. The disease is epidemiologically associated with the use of an inactivated bovine virus diarrhoea (BVD) vaccine and is currently considered to be caused by absorption of colostral antibody produced by some vaccinated cows ("BNP dams"). Alloantibodies capable of binding to the leukocyte surface have been detected in BNP dams and antibodies recognising bovine MHC class I and ß-2-microglobulin have been detected in vaccinated cattle. In this study, calves were challenged with pooled colostrum collected from BNP dams or from non-BNP dams and their bone marrow hematopoietic progenitor cells (HPC) cultured in vitro from sternal biopsies taken at 24 hours and 6 days post-challenge. RESULTS: Clonogenic assay demonstrated that CFU-GEMM (colony forming unit-granulocyte/erythroid/macrophage/megakaryocyte; pluripotential progenitor cell) colony development was compromised from HPCs harvested as early as 24 hour post-challenge. By 6 days post challenge, HPCs harvested from challenged calves failed to develop CFU-E (erythroid) colonies and the development of both CFU-GEMM and CFU-GM (granulocyte/macrophage) was markedly reduced. CONCLUSION: This study suggests that the bone marrow pathology and clinical signs associated with BNP are related to an insult which compromises the pluripotential progenitor cell within the first 24 hours of life but that this does not initially include all cell types.