RESUMO
Comparative quantitative experiments were designed to study the expression of H-2Kd and H-2Dd antigens on three different leukemia cell lines induced by Gross murine leukemia virus (MuLV)in BALB/c (H-2d) mice. The H-2 restriction patterns of syngeneic cytolytic T lymphocytes (CTL) directed against Gross MuLV-induced tumors were correlated with these quantitations of H-2Kd and H-2Dd antigens, Our results obtained by quantitative absorption of monospecific antisera indicated that the three BALB/c tumor cell lines expressed different amounts of H-2Kd and H-2Dd antigens, with H-2Dd antigen showing the greatest variability in expression because it ranged from barely detectable levels to one-eighth the amount of H-2Dd antigen expressed on normal BALB/c spleen cells. The H-2 restriction patterns of Gross MuLV-specific CTL were directly affected by these quantitative modulations in the expression of H-2Kd and H-2Dd antigens, as revealed by three independent approaches: (a) inhibition of CTL activity by monospecific anti-H-2 sera in the absence of complement; (b)competitive inhibition of CTL-mediated cytotoxicity by the addition of excess tumor cells into the reaction mixture; and (c) analysis of CTL specificities using cloned CTL populations. Our results thus indicate that H-2 restriction of tumor-specific CTL activity can be directed at the target cell level by variations in the expression of H-2 antigens.
Assuntos
Citotoxicidade Imunológica , Antígenos H-2 , Leucemia Experimental/imunologia , Linfócitos T/imunologia , Vírus AKR da Leucemia Murina/imunologia , Animais , Antígenos de Neoplasias , Ligação Competitiva , Transformação Celular Neoplásica , Proteínas do Sistema Complemento , Epitopos , Soros Imunes/farmacologia , Leucemia Experimental/etiologia , Camundongos , Camundongos Endogâmicos BALB C , Camundongos Endogâmicos C57BLRESUMO
Cytolytic T lymphocytes (CTL) specific for the virus-induced and leukemia-associated Friend, Moloney, Rauscher (FMR) antigen are easily detected in the spleens of primary and secondary stimulated H-2b or H-2d mice. They react, respectively, with H-2Db + FMR and H-2Kd + FMR; Dd and Kb never being involved. On the other hand, recombinant (KbDd) mice are relatively low responders that produce CTL only after secondary stimulation. Competition and blocking experiments with monospecific anti-H-2 antibodies have demonstrated that on the same H-2b tumor cells, C57BL/6 (H-2b) lymphocytes recognize Db + FMR, whereas B10.A(5R) lymphocytes recognize Kb + FMR, the restriction cannot, therefore be explained by a specific association of viral molecules with certain H-2 products. The CTL response of (B10 X 5R)F1 hybrids is (a) easily detected in primary reaction, the high responder anti-FMR phenotype being dominant and (b) directed against Db + FMR, F1 mice being low responder against Kb + FMR like the B10 parent. These results suggest that a D region-associated immune response gene controls the cell-mediated anti-FMR reaction, the best available H-2 + FMR antigenic association being chosen by CTL precursors.
Assuntos
Antígenos de Neoplasias , Citotoxicidade Imunológica , Genes MHC da Classe II , Antígenos H-2 , Células Matadoras Naturais/imunologia , Leucemia Experimental/imunologia , Animais , Antígenos Virais , Imunidade Celular , Memória Imunológica , Linfoma/imunologia , Camundongos , Vírus da Leucemia Murina de Moloney/imunologiaRESUMO
The physical association of 40 antigenic peptides and purified HLA class I and class II molecules was monitored using a direct peptide binding assay (PBA) in solid phase and an inhibition peptide binding assay (IPBA) in which the competing peptide was present in a soluble phase. We also examined the ability of different peptides to inhibit the lytic activity of human antiviral cytolytic T cells towards cells incubated with the corresponding target peptide. Our results showed that: (a) Binding of a given human T cell-recognized peptide to several HLA class I and class II molecules occurred frequently. Nevertheless, preferential binding of peptides to their respective restriction molecules was also observed. (b) Binding of HLA molecules to peptides recognized by murine T cells occurred less frequently. (c) 11 of 24 (46%) randomly selected HIV-1 peptides contained agretopic residues allowing their binding to HLA molecules. (d) The kinetics of HLA/peptide association depended on the peptide tested and were faster than or similar to those reported for Ia molecules. Dissociation of these complexes was very low. (e) Peptide/HLA molecule binding was dependent on length, number of positive charges, and presence of hydrophobic residue in the peptide. (f) A correlation was demonstrated between a peptide inhibitory effect in the IPBA and its blocking effect in the cytolytic test. Our data indicated that the restriction phenomenon observed in T cell responses was not strictly related to either an elective HLA/peptide association, or a high binding capacity of a peptide to HLA molecules. These data also showed that the PBA and IPBA are appropriate for the detection of agretopic residues within HIV-1 proteins.
Assuntos
Complexo Antígeno-Anticorpo , Antígenos Virais/imunologia , HIV-1/imunologia , Antígenos HLA , Linfócitos T Citotóxicos/imunologia , Proteínas Virais/imunologia , Sequência de Aminoácidos , Especificidade de Anticorpos , Antígenos de Histocompatibilidade Classe I , Antígenos de Histocompatibilidade Classe II , Humanos , Dados de Sequência Molecular , Peptídeos/síntese químicaRESUMO
It was demonstrated previously that the cytolysis of murine viral lymphoma cells by anti-murine sarcoma virus (MSV) syngeneic T-killer lymphocytes was restricted by some products of the H-2 complex. The respective role of the products of different regions of the H-2 complex were studied with six H-2(b) and three H-2(d) lymphomas induced by five different type C viruses. They were tested in a classical chromium release test against anti-MSV T-killer cells obtained from different inbred strains of mice, including several H-2 recombinants. Tumors o pound the H-2(b) haplotype were lysed only when effectors and target cells have in common the D(b) region. On the contrary an identity limited to the K end of the H-2 complex is necessary and sufficient in the H-2(d) haplotype. An in vitro restimulation of the spleen cells with concanavalin A strongly increased the activity of in vivo-primed T lymphocytes but did not provide any response for in vivo-primed but nonresponder cells. Preincubation of the tumor cells with anti-H-2 sera abolished the lysis by syngeneic anti-MSV effector lymphocytes. The same results were obtained by preincubating the H-2(b) targets with anti-H-2D(b), or the H-2(d) target with anti-H-2K(d). Preincubation with anti-H-2K(b) or anti- H-2D(d) were ineffective. These results show that the T-killer/target cells interaction in the MSV system involved some products of the H-2 complex which might be different with the various H-2 haplotypes and could possibly vary according to the antigenic specificity. A specific association of a viral product with a normal cellular structure, directed by the H-2 region during the viral budding could explain the observed results.
Assuntos
Antígenos Virais , Gammaretrovirus/imunologia , Antígenos de Histocompatibilidade , Imunidade Celular , Linfoma/imunologia , Vírus do Sarcoma Murino/imunologia , Linfócitos T/imunologia , Animais , Reações Antígeno-Anticorpo , Testes Imunológicos de Citotoxicidade , Genes , Ligação Genética , Isoanticorpos , Camundongos , Camundongos Endogâmicos , Neoplasias Experimentais/imunologia , Baço/imunologiaRESUMO
Human immunodeficiency virus (HIV) induces strong responses from human histocompatibility leukocyte antigen (HLA) class I-restricted cytotoxic T lymphocytes (CTL). In a previous report we identified an immunodominant region (amino acids 73-144) in the NEF protein that was recognized by CD8+ class I-restricted CTL of most asymptomatic individuals. Analysis of the 73-144 region by peptide sensitization, experiments using overlapping peptides corresponding to the LAI isolate identified the peptide sequences located between residues 73 and 82 or 84 and 92 and the peptide sequence between residues 134 and 144 as cognate peptides for HLA-A11- and HLA-B18-restricted epitopes, respectively. This report describes the variable demonstrable reactivities of CTL obtained from HLA-A11 or HLA-B18 seropositive, asymptomatic patients who all had a response to the virus NEF protein, but who did not always recognize appropriate cognate peptides. The high mutation rate of HIV probably facilitates the selection of mutants that can avoid the cellular immune response. We therefore analyzed the variability of these epitopes restricted by HLA-A11 and HLA-B18. We sequenced several viral isolates from HLA-A11 and HLA-B18 donors who recognized certain HLA-peptide complexes and from those who did not. A CTL sensitization assay was used to show that some mutations led to a great reduction in CTL activity in vitro. This might be due to failure of the mutated epitope to bind major histocompatibility complex class I molecule. A simple assay was used to detect peptides that promoted the assembly of class I molecules. Some of these mutations at major anchor positions prevented HLA-A11/peptide binding, and consequently impaired recognition of the HLA-peptide complex by the T cell receptor.
Assuntos
Epitopos/genética , Produtos do Gene nef/imunologia , HIV-1/imunologia , Mutação , Linfócitos T Citotóxicos/imunologia , Sequência de Aminoácidos , Sequência de Bases , Produtos do Gene nef/genética , HIV-1/genética , Antígenos HLA-A/fisiologia , Antígeno HLA-A11 , Antígenos HLA-B/fisiologia , Antígeno HLA-B18 , Humanos , Dados de Sequência Molecular , Produtos do Gene nef do Vírus da Imunodeficiência HumanaRESUMO
A helper-independent Friend leukemia virus was used to infect bone marrow cultures. This virus induces myeloblastic leukemia in mice after a long latency period. Infection of the bone marrow cultures resulted in the in vitro production of myeloblastic leukemogenesis after a long latency period. Three steps were observed in the evolution of the infected cultures, and permanent cell lines were derived at each step. This allowed us to individualize three successive events in the course of the myeloblastic transformation: (i) an abnormal responsiveness to the physiological hormone granulo-macrophagic colony-stimulating factor, (ii) the acquisition of growth autonomy, and (iii) the acquisition of in vivo tumorigenicity.
Assuntos
Leucemia Mieloide Aguda/etiologia , Animais , Medula Óssea , Transformação Celular Neoplásica , Transformação Celular Viral , Células Cultivadas , Modelos Animais de Doenças , Vírus da Leucemia Murina de Friend , CamundongosRESUMO
Over two-thirds of the current gene therapy protocols use retroviral gene transfer systems. We have developed an efficient retroviral-based method that allows rapid identification of gene transfer in living mammalian cells. Cells were generated containing a gene for an improved (humanized, red-shifted) version of the Aequorea victoria green fluorescent protein (hRGFP) from a retroviral vector. The hRGFP gene was used to produce an amphotropic vector producer cell line that demonstrated vibrant green fluorescence after excitation with blue light. A375 melanoma cells transduced with the retroviral vector demonstrated stable green fluorescence. Both PA317 murine fibroblasts and A375 human cell lines containing the vector were easily detected by FACS analysis. These vectors represent a substantial improvement over currently available gene transfer marking systems. Bright, long-term expression of the hRGFP gene in living eukaryotic cells will advance the study of gene transfer, gene expression, and gene product function in vitro and in vivo particularly for human gene therapy applications.
Assuntos
Expressão Gênica , Técnicas de Transferência de Genes , Proteínas Luminescentes/química , Proteínas Luminescentes/genética , Animais , Sequência de Bases , Biotecnologia , Separação Celular , Primers do DNA/genética , Citometria de Fluxo , Fluorescência , Terapia Genética , Vetores Genéticos , Proteínas de Fluorescência Verde , Humanos , Camundongos , Retroviridae/genética , Células Tumorais CultivadasRESUMO
Peripheral blood lymphocytes (PBL) and epidermal cells (EC) of 44 patients to be grafted with bone marrow from an HLA-identical sibling have been used as stimulator cells in primary cultures with effector PBL of one or several potential donors. Proliferative responses against PBL did not differ from those obtained with effector cells cultured in medium alone, whereas EC induced clearly positive proliferation in 21/53 (40%) of the pairs tested. Evaluation of 30 patients followed for more than 3 months after the graft shows that a high level of response in the mixed epidermal cell lymphocyte reaction is directly correlated with the incidence of acute graft-versus-host disease.
Assuntos
Transplante de Medula Óssea , Epiderme/imunologia , Doença Enxerto-Hospedeiro/etiologia , Teste de Histocompatibilidade/métodos , Leucemia/terapia , Linfócitos/imunologia , Doença Aguda , Doença Enxerto-Hospedeiro/imunologia , Antígenos HLA/imunologia , HumanosRESUMO
The XC infectious center assay was used to study the nature of the lymphoid cells producing N-tropic C-type viruses in preleukemic AKR mice. Viral production by thymic cell suspensions was very low and was possibly due to contaminating cells. Production at least 100-fold higher was found in spleen cells and was probably due to non-T-cells. The significance of these results is discussed briefly, including the possibility that the N-tropic XC syncitia-inducing type C virus of young AKR mice is not the leukemogenic agent.
Assuntos
Vírus AKR da Leucemia Murina , Vírus da Leucemia Murina , Leucemia Experimental/microbiologia , Linfócitos/microbiologia , Pré-Leucemia/microbiologia , Replicação Viral , Animais , Camundongos , Camundongos Endogâmicos AKR , Baço/microbiologia , Linfócitos T/microbiologia , Timo/microbiologia , Infecções Tumorais por Vírus/microbiologiaRESUMO
To identify HIV peptides containing HLA class I binding regions, different studies have been performed. These include the detection of interactions between HIV peptides and purified HLA molecules in solid-phase assays, the measurement of HLA molecule assembly in the presence of peptide added to cell lysates, and the detection of inhibition of CTL-mediated cytolysis by competition between peptides on target cells. To date, the HIV epitopes recognized by anti-HIV CTL are from the Env, Gag, Nef, and Pol proteins and they are identified using synthetic peptides of 12 to 20 amino acids. The search for a correlation between known HIV CTL epitopes and the results of HLA/peptide interaction assays reveals that: (1) most of the peptides that are positive in the assembly assay contain a HLA-A2 peptide motif but the correlation between these positive peptides and the CTL epitopes is not obvious; (2) a high proportion of HIV epitopes are included in the peptides positive in solid-phase binding and in inhibition of cytolysis assays, although these tests do not allow us to predict HLA restriction; (3) the HLA-A2 peptide motif is not systematically included in HLA-A2-restricted CTL epitopes, this observation raising the possibility that other sequences are involved in HLA binding.
Assuntos
Sítios de Ligação/imunologia , Epitopos/imunologia , HIV-1/imunologia , Antígenos de Histocompatibilidade Classe I/imunologia , Proteínas dos Retroviridae/imunologia , Alelos , Sequência de Aminoácidos , Humanos , Imunoensaio , Dados de Sequência Molecular , Peptídeos/imunologia , Linfócitos T Citotóxicos/imunologiaRESUMO
The HLA-B7 and HLA-A11 molecules expressed on murine transfectants have been analysed by one- and two-dimensional polyacrylamide gel electrophoresis (PAGE). Two different murine cells, L and P815-HTR have been compared, because it has been previously established that P815 transfectants were much more sensitive to human cytolytic cells than L transfectants. Three kinds of HLA molecules were present on these cells: (1) normal HLA molecules with 2D-PAGE profiles identical to those of the molecules isolated from human cells; (2) HLA molecules of usual size but with more various charges than HLA molecules detected on human cells. This heterogeneity was constantly found with cells expressing HLA-B7 or -A11 antigens, both in L and in P815 transfectants, including several clones. These forms were detected by anti-HLA monoclonal antibodies and by antipeptide (from HLA-B7) antibodies; (3) other unusual products corresponding to shorter heavy chains: molecules of various mol. wts and charges were detected in HLA-B7 but not in HLA-A11 transfectants. They were observed using antipeptide sera but were not seen with anti-HLA monoclonal antibodies. These products were possibly related to the DNA used for transfection and it cannot be excluded that such abnormalities only detectable by antipeptide sera would exist in other transfectants. The functional discrepancies between P815 and L transfectants cannot be clearly explained by these biochemical results.
Assuntos
Genes , Antígenos HLA/análise , Antígenos HLA-A , Transfecção , Animais , Linhagem Celular , Eletroforese em Gel de Poliacrilamida , Antígenos HLA/genética , Antígeno HLA-A11 , Antígeno HLA-B7 , Herpesvirus Humano 4/genética , Humanos , Células L , Camundongos , Peso Molecular , Neuraminidase/farmacologiaRESUMO
The expression of a 20 alpha-hydroxysteroid dehydrogenase (20 alpha SDH) activity was investigated in various murine hematopoietic cells. Large differences appeared between cells belonging to the same hematopoietic lineage. Normal thymocytes were positive when splenocytes, B and T lymphoma cell lines were negative. In two stromal fibroblastic cell lines, the expression of 20 alpha SDH was very high, whereas it was negative in NIH/3T3 normal fibroblasts. Among myelomonocytic cell lines, six expressed high levels and two were negative. Contaminating lymphoid subpopulations were not detectable in these cell lines. The levels of detected enzymatic activity seemed unrelated with the virus infection. The presence of 20 alpha SDH activity in factor-independent myelomonocytic cell lines, and the lack of induction of the enzymatic activity by the IL-3 containing WEHI-3B conditioned medium in negative cell lines, led us to suggest that myelomonocytic cells intrinsically express the 20 alpha SDH enzymatic activity, as well as other hemopoietic and stromal cell lines.
Assuntos
20-Hidroxiesteroide Desidrogenases/metabolismo , Células-Tronco Hematopoéticas/enzimologia , Animais , Linhagem Celular , Fibroblastos/citologia , Fibroblastos/enzimologia , Substâncias de Crescimento/metabolismo , Células-Tronco Hematopoéticas/citologia , Cinética , Tecido Linfoide/citologia , Tecido Linfoide/enzimologia , Linfoma/enzimologia , Camundongos , Camundongos Endogâmicos BALB C , Camundongos Endogâmicos C57BL , Linfócitos T/citologia , Linfócitos T/enzimologiaRESUMO
OBJECTIVES: To determine whether cytotoxic T lymphocytes have a beneficial effect during infection with the simian immunodeficiency virus (SIV) in macaques. DESIGN AND METHODS: We followed up 12 rhesus macaques experimentally infected with SIV. Cytotoxic T lymphocytes were detected in nine macaques, who were subdivided into a group of high responders (n = 6), with a sustained and polymorphic response directed against most SIV proteins, and a second group of weak responders (n = 3), in which the responses were only transient and directed against only a few proteins. A third group was characterized by the absence of any cytotoxic T-lymphocyte response (n = 3). Proliferative responses closely paralleled cytotoxic responses in intensity and evolution. RESULTS: Clinical profiles and CD4 cell counts were markedly linked to cytotoxic activity; five out of six macaques that responded to multiple proteins were still healthy 2 years after SIV infection, with two of them presenting a decrease in circulating CD4 cells concomitant with the disappearance of the cytotoxic T-lymphocyte response. Conversely, five non-responder or weak-responder macaques developed overt disease after 4-21 months. CONCLUSIONS: These data suggest that a cytotoxic response may predict a better clinical outcome.
Assuntos
Síndrome de Imunodeficiência Adquirida dos Símios/imunologia , Vírus da Imunodeficiência Símia/imunologia , Linfócitos T Citotóxicos/imunologia , Animais , Antígenos Virais/imunologia , Linfócitos T CD4-Positivos/imunologia , Antígenos CD8/metabolismo , Linhagem Celular , Contagem de Leucócitos , Ativação Linfocitária , Macaca mulatta , Proteínas dos Retroviridae/imunologia , Síndrome de Imunodeficiência Adquirida dos Símios/sangue , Fatores de TempoRESUMO
OBJECTIVE: To carry out, within France, a large-scale molecular epidemiological investigation on the principal neutralizing determinant of HIV-1, located in the third variable region (V3) of the envelope protein. Such investigations are of the utmost importance in the identification and monitoring of the distribution and spread of different viral strains internationally. DESIGN: Using polymerase chain reaction (PCR), we examined the genetic variation of the V3 region sequences of 28 HIV-infected patients from Paris, France. RESULTS: Comparison of the Parisian V3 loop sequences with other published data indicates that the range of diversity in France is included within that of a large group that contains sequences from North America, the rest of Europe, Japan, India and Africa. Variability appears to be lower in the V3 loop than in its flanking regions. Five out of the six putative N-linked glycosylation sites show preferential alterations to charged amino acids. We report two motifs at the tip of the loop that have not been described previously. CONCLUSIONS: The structural homogeneity and the wide geographic representation of the major V3 group suggests that a common strategy could be applied to a large proportion of isolates in the development of a broad-spectrum HIV vaccine.
Assuntos
Síndrome da Imunodeficiência Adquirida/microbiologia , Proteína gp120 do Envelope de HIV/genética , HIV-1/genética , Fragmentos de Peptídeos/genética , Síndrome da Imunodeficiência Adquirida/epidemiologia , Sequência de Aminoácidos , Sequência de Bases , Primers do DNA , Variação Genética , Glicosilação , Proteína gp120 do Envelope de HIV/classificação , Humanos , Dados de Sequência Molecular , Paris/epidemiologia , Fragmentos de Peptídeos/classificação , Reação em Cadeia da Polimerase , Homologia de Sequência de AminoácidosRESUMO
OBJECTIVE: To study the degree of immunogenicity of each HIV-1 protein. DESIGN: In most viral systems, antiviral cytotoxic T-lymphocytes (CTL) from a given donor preferentially recognize only one or a small number of viral proteins. METHODS: Anti-HIV CTL were generated by in vitro stimulation of peripheral blood mononuclear cells from seropositive donors and tested against multiple HIV-1 proteins or groups of proteins encoded by seven genes (env, gag, pol, nef, rev, tat and vif). Using autologous target cells infected with recombinant vaccinia viruses expressing one of the HIV-1LAI proteins, we compared the cytolytic activities obtained from bulk culture with those found in limiting dilution analysis (LDA). RESULTS: Our results were noteworthy for the following reasons. (1) Each responding donor reacted simultaneously to multiple proteins; this is very unusual in other viral systems. Anti-Gag CTL were detected in most, and anti-Pol in approximately three-quarters, of the patients, together with very high amounts of the corresponding CTL precursors in LDA. CTL against Env and Nef were found in two-thirds of the patients, while Vif- and Rev-specific CTL were less frequent. Finally, Tat was seldom recognized by CTL, but its antigenicity was revealed in LDA. (2) All responding cells revealed in bulk cultures as well as in LDA were CD8+ T-cells, and their in vitro differentiation did not require the help of CD4+ T-cells. (3) Proteins from the HIV-1LAI isolate were recognized with high frequency by CTL from seropositive donors, most certainly being infected by other isolates, which suggests that relatively conserved epitopes are predominant targets of CTL. CONCLUSION: Taken together, these results are encouraging for vaccine purposes, since anti-HIV-1 CTL stimulation is thought to be a requirement for such a vaccine.
Assuntos
HIV-1/imunologia , Proteínas dos Retroviridae/imunologia , Linfócitos T Citotóxicos/imunologia , Vacinas contra a AIDS/imunologia , Testes Imunológicos de Citotoxicidade , Citotoxicidade Imunológica , Soropositividade para HIV/imunologia , HIV-1/genética , Humanos , Técnicas In Vitro , Proteínas dos Retroviridae/genética , Subpopulações de Linfócitos T/imunologiaRESUMO
OBJECTIVE: Test the efficacy of a mixture of six NEF (N1, N2, N3), GAG (G1, G2) and ENV (E) lipopeptides in the induction of B- and T-cell anti-HIV responses. DESIGN: A randomized phase I open-label dose-finding trial. Twenty-eight healthy seronegative volunteers received the lipopeptides, with or without the adjuvant QS21. METHODS: Anti-HIV-peptide antibodies were detected by enzyme-linked immunosorbent assay and Western blotting. Induction of cellulary responses was assessed by proliferative test and (51)Cr-release assay. RESULTS: Local and systemic adverse reactions were always mild or moderate. After three injections an antibody response was detected in 25 out of 28 volunteers (89%). T cells from 19 (79%) of the 24 volunteers proliferated in response to at least one peptide. The majority of the volunteers had induced a multispecific proliferative response; that is, cells from volunteers proliferated to two (five of 19), three (five of 19), four (three of 19) or five peptides (one of 19). Cytotoxic responses by anti-HIV CD8+ lymphocytes could be tested in 24 volunteers, 13 (54%) of whom had clear and reproducible responses, with strong activity in the remaining 12 (> 20% of specific lysis), and polyepitopic responses were detected in at least seven of the 13 responders. Cytotoxic responses were found against the whole NEF protein (clade B LAI) in three of four tested volunteers and cross-reactions with the proteins of clade B (MN) and clade A (Bangui) HIV-1 strains, and also HIV-2 ROD, were detected in one of two tested volunteers. CONCLUSIONS: Lipopeptides are promising immunogens for an AIDS vaccine.
Assuntos
Vacinas contra a AIDS/administração & dosagem , Produtos do Gene nef/química , Soronegatividade para HIV/imunologia , Lipoproteínas/administração & dosagem , Fragmentos de Peptídeos/administração & dosagem , Vacinas contra a AIDS/efeitos adversos , Vacinas contra a AIDS/imunologia , Adulto , Sequência de Aminoácidos , Ensaio de Imunoadsorção Enzimática , Feminino , Anticorpos Anti-HIV/sangue , Humanos , Lipoproteínas/efeitos adversos , Lipoproteínas/química , Lipoproteínas/imunologia , Masculino , Pessoa de Meia-Idade , Dados de Sequência Molecular , Fragmentos de Peptídeos/efeitos adversos , Fragmentos de Peptídeos/química , Fragmentos de Peptídeos/imunologia , Linfócitos T Citotóxicos/imunologiaRESUMO
This study will evaluate the safety and efficacy of allogenic donor lymphocyte infusions in patients who have relapsed hematologic malignancies after allogeneic bone marrow transplantation (BMT). Donor lymphocyte transfusions have resulted in the cure of some patients with relapsed leukemia or lymphoproliferative disorder after allogeneic BMT, but has been complicated by the development of graft versus host disease (GvHD). We hypothesize that a retroviral vector containing the Herpes simplex thymidine kinase (HStk) gene will allow for retention of the anti-leukemia response of transfused donor lymphocytes while allowing for the adverse effects of GVHD to be mitigated. Patients with relapsed hematologic malignancies after allogeneic BMT will be infused with ex vivo gene modified donor lymphocytes. The Herpes Simplex thymidine kinase (HStk) gene will be transduced into the cells ex vivo using LTKOSN. 1 vector supernate. Insertion of the HStk gene into lymphocytes confers a sensitivity to the anti-herpes drug ganciclovir (GCV). This selective destruction of donor lymphocytes in situ will be used to abrogate the effect of graft versus host disease, if it develops.
Assuntos
Protocolos Clínicos , Imunoterapia Adotiva/métodos , Leucemia Linfoide/terapia , Timidina Quinase/genética , Estudos de Avaliação como Assunto , Vetores Genéticos , Humanos , Imunoterapia Adotiva/efeitos adversos , Linfócitos/citologia , Linfócitos/metabolismo , Seleção de Pacientes , Indução de Remissão/métodos , Simplexvirus/enzimologia , Timidina Quinase/metabolismoRESUMO
Lymphoma cells induced in vivo by exogenous C type viruses are usually used as target cells to test the activity of cytolytic T lymphocytes (CTL) directed against the virus-induced cell surface FMR antigen. Such lymphomas are available only in a small number of inbred strains of mice, thus setting limits to the study of H-2 antigens in the interaction between CTL and tumor target cells. A method is proposed to overcome this, using mitogen-induced blast cells from adult mice neonatally infected with C type viruses. Such blast cells bear serologically detectable viral antigens and function as convenient targets in the chromium release test, as well as competitor cells or stimulator cells in vitro. With this method it has been possible to study T cell-mediated anti-FMR reactions in 12 different inbred strains of mice bearing 10 different H-2 haplotypes. The same method could probably be used in any inbred strain, greatly improving the possibility of immunogenetic studies in C type virus systems.
Assuntos
Citotoxicidade Imunológica , Técnicas Imunológicas , Linfoma/imunologia , Linfócitos T/imunologia , Animais , Transformação Celular Viral , Ativação Linfocitária , Camundongos , Camundongos Endogâmicos BALB C/imunologia , Camundongos Endogâmicos C57BL/imunologia , Camundongos Endogâmicos/imunologia , Mitógenos/farmacologia , RetroviridaeRESUMO
An ELISA detecting anti-HLA antibodies of rabbit, mouse or human origin was developed using plates coated with HLA molecules purified on affinity columns. The sensitivity of the assay was optimal when coating was performed in PBS, pH 7.8 at 4 degrees C for 6-16 h and using a serum incubation period of 16 h at 4 degrees C. The optimum protein concentration for coating was estimated to be 1 micrograms/ml. With monoclonal anti-HLA sera, antipeptide antibodies from mice or rabbit and human alloantisera, this method appeared to be highly sensitive, very specific and reproducible.
Assuntos
Antígenos HLA/análise , Animais , Anticorpos Monoclonais/imunologia , Relação Dose-Resposta Imunológica , Ensaio de Imunoadsorção Enzimática/métodos , Humanos , Concentração de Íons de Hidrogênio , Isoanticorpos/imunologia , Camundongos , Oligopeptídeos/imunologia , Coelhos , Temperatura , Fatores de TempoRESUMO
A cellular radioimmunoassay utilizing 125I-labelled Protein A was used for detecting antigen-antibody complexes on glutaraldehyde fixed cells attached to microtiter plates. This method is rapid, sensitive and specific for revealing H-2 private and public specificities as well as Ia and Lyt antigens. As plates may be kept for months, several reactivities can be tested in one step on a large panel rendering a regular supply of animals unnecessary.