RESUMO
We explored the expression of the interleukin 2 receptor (IL-2R) and the synthesis of IL-2R messenger RNA by peripheral blood leukocytes obtained from medical students experiencing examination stress in three independent studies. The peripheral blood leukocytes obtained at low-stress baseline periods had significantly higher percentages of IL-2R-positive cells when compared with cells obtained from the same individuals during examinations. In addition, IL2-R messenger RNA in peripheral blood leukocytes decreased significantly during examination periods in a subset of 13 subjects. In one study, we found an increase in the accumulation of interleukin 2 in cultures of cells showing down regulation of IL-2R expression and IL-2R messenger RNA levels. While there are ample data demonstrating stress-associated decrements in the immune response in humans and animals, these data provide the first evidence that this interaction may be observed at the level of gene expression. The data suggest one mechanism whereby the central nervous system modulates the immune response during psychological stress.
Assuntos
Expressão Gênica/fisiologia , Interleucina-2/biossíntese , Leucócitos/imunologia , Receptores de Interleucina-2/imunologia , Estresse Psicológico/imunologia , Adulto , Células Cultivadas , Regulação para Baixo/fisiologia , Feminino , Humanos , Leucócitos/metabolismo , Ativação Linfocitária , Masculino , RNA Mensageiro/metabolismo , Receptores de Interleucina-2/genética , Receptores de Interleucina-2/metabolismo , Estresse Psicológico/metabolismoRESUMO
Lymphoid tissues are extensively innervated by noradrenergic fibers of the sympathetic nervous system. 6-hydroxydopamine (6-OHDA)-induced chemical sympathectomy is commonly used to assess the impact of this innervation on immune function. Using the glucocorticoid receptor antagonist RU486, the mineralocorticoid receptor antagonist spironolactone, and the beta-adrenergic receptor antagonist nadolol, the roles of corticosterone and norepinephrine in sympathectomy-mediated modulation of both the primary and memory cellular immune responses to herpes simplex virus type 1 (HSV-1) infection was investigated. We demonstrated that both of these immunomodulators play a role in mediating sympathectomy-induced suppression of the generation of HSV-specific primary cytotoxic T lymphocytes (CTL) and the activation of HSV-specific memory CTL (CTLm). Furthermore, we demonstrated a role for both Type I and Type II corticosteroid receptors in the regulation of HSV-specific immunity. Overall, these findings not only further support a role for neuroendocrine-mediated modulation of immune function, but also a need to exercise caution in attributing the effects of chemical sympathectomy to solely the absence of sympathetic innervation of lymphoid tissues.
Assuntos
Herpes Simples/imunologia , Herpesvirus Humano 1 , Simpatectomia Química , Linfócitos T Citotóxicos/imunologia , Linfócitos T Citotóxicos/virologia , Animais , Linhagem Celular , Corticosterona/imunologia , Antagonistas de Hormônios/farmacologia , Ativação Linfocitária/efeitos dos fármacos , Ativação Linfocitária/imunologia , Masculino , Camundongos , Camundongos Endogâmicos C57BL , Mifepristona/farmacologia , Neuroimunomodulação/efeitos dos fármacos , Neuroimunomodulação/imunologia , Norepinefrina/imunologia , Oxidopamina , Receptores de Mineralocorticoides/imunologia , Receptores de Esteroides/imunologia , Baço/imunologia , Baço/virologia , SimpatolíticosRESUMO
Adoptive immunotherapy represents a potentially effective approach by which to control the extent of viral infections in an immunocompromised host. However, the impact of psychological stress and its associated neuroendocrine components on the efficacy of such a treatment strategy has yet to be determined. In the studies described herein, we have developed and utilized a model of primary, local herpes simplex virus (HSV) infection in radiation-induced, immunosuppressed C57BL/6 mice to investigate the role of stress in altering the protective capacity of adoptively transferred lymphocytes that contribute to the resolution of primary HSV infection. The sublethal dose of irradiation chosen for this model was shown to abrogate the local, adaptive immune response to HSV infection as measured by the degree of in vivo lymphoproliferation, development of HSV-specific cytotoxic T lymphocytes (CTL), and production of gamma interferon (IFN-gamma). Both short- and long-term acute stress, applied in the form of physical restraint, diminished the effectiveness of adoptively transferred lymphocytes as was indicated by an enhancement of viral replication in the footpad tissue and an increased rate of mortality. A reduction in the levels of IFN-gamma at the site of primary HSV infection represented at least one mechanism underlying this suppression of anti-viral immunity. Furthermore, the time-dependent restoration of immune function following irradiation was shown to be compromised in mice subjected to the restraint stress procedure. Together, these findings emphasize the potential role of psychological stress in suppressing both the capability of adoptive immunotherapeutic procedures to combat viral infection and the reestablishment of immune function in individuals who have undergone immunosuppressive therapy.
Assuntos
Transferência Adotiva , Herpes Simples/terapia , Hospedeiro Imunocomprometido/imunologia , Imunoterapia , Simplexvirus/imunologia , Estresse Psicológico/imunologia , Animais , Formação de Anticorpos/efeitos da radiação , Especificidade de Anticorpos , Pé , Herpes Simples/imunologia , Herpes Simples/mortalidade , Interferon gama/metabolismo , Linfonodos/patologia , Linfonodos/fisiopatologia , Linfócitos/fisiologia , Masculino , Camundongos , Camundongos Endogâmicos C57BL , Restrição Física , Fatores de Tempo , Irradiação Corporal TotalRESUMO
A murine model of herpes simplex virus (HSV) infection was used to examine the role of the adrenal gland in restraint stress-induced suppression of viral immunity. Adrenal-dependent mechanisms were important for suppressing the generation of HSV-specific cytotoxic T lymphocytes (CTL) but not the associated diminished lymphadenopathy in response to local HSV infection. While exogenous corticosterone administration alone was unable to suppress lymphadenopathy and CTL generation in adrenalectomized mice, an adrenal-independent mechanism induced by restraint stress functioned in synergy with corticosterone to suppress lymphadenopathy and CTL development. These results suggest that both adrenal-dependent and independent mechanisms contribute to stress-induced modulation of HSV immunity.
Assuntos
Glândulas Suprarrenais/imunologia , Herpes Simples/imunologia , Imunidade Celular , Estresse Fisiológico/imunologia , Adrenalectomia , Animais , Corticosterona/sangue , Corticosterona/farmacologia , Masculino , Camundongos , Linfócitos T Citotóxicos/imunologiaRESUMO
We have previously demonstrated in a murine model system that psychological stress, applied in the form of physical restraint, suppresses both the activation of splenic-derived, herpes simplex virus (HSV)-specific memory cytotoxic T-lymphocytes (CTLm) to the lytic phenotype and the production of cytokines associated with CTL activation and function. In the studies described herein, we investigated the hypothesis that an adrenal-dependent event is responsible, either in whole or in part, for these observations. While adrenalectomy was shown to abrogate stress-induced suppression of both HSV-specific CTLm activation and the production of IL-6 and IFN-gamma, the reduction in splenic cellularity associated with restraint stress remained, In addition, a role for adrenal function in the regulation of splenic cellularity and IFN-gamma production in non-stressed mice was observed. Together, these results indicate that both adrenal-dependent and adrenal-independent events, operative under both baseline and stress conditions, mediate control of the memory component of the cellular immune response to HSV infection. Overall, these studies provide insight into the mechanisms by which psychological stress modulates immune responsiveness to viral pathogens.
Assuntos
Glândulas Suprarrenais/fisiopatologia , Memória Imunológica/fisiologia , Simplexvirus/imunologia , Estresse Psicológico/fisiopatologia , Linfócitos T Citotóxicos/fisiologia , Adrenalectomia , Animais , Interferon gama/metabolismo , Interleucina-6/metabolismo , Masculino , Camundongos , Camundongos Endogâmicos C57BL , Baço/patologia , Linfócitos T Citotóxicos/imunologiaRESUMO
Physical restraint administered to C57BL/6 mice significantly altered the inflammatory response to influenza virus infection and depressed anti-viral cellular immunity. Restraint-stressed animals showed a pattern of reduced mononuclear cell infiltration and lung consolidation which coincided with elevated plasma corticosterone levels. Furthermore, cellular immunity to virus was significantly depressed; interleukin-2 secretion was reduced by 96% and 59% in the mediastinal lymph nodes and spleens, respectively, as compared to a non-restrained group. However, the magnitude of the humoral immune response to influenza virus was unaffected by restraint stress. Anti-viral IgG antibody levels in restrained/infected mice did not differ when compared to a non-restrained/infected control group 14 days post-infection.
Assuntos
Infecções por Orthomyxoviridae/imunologia , Estresse Fisiológico/imunologia , Animais , Anticorpos Antivirais/biossíntese , Corticosterona/sangue , Imunoglobulina G/biossíntese , Interleucina-2/biossíntese , Masculino , Camundongos , Camundongos Endogâmicos C57BL , Infecções por Orthomyxoviridae/patologia , Restrição Física , Linfócitos T Auxiliares-Indutores/imunologiaRESUMO
Mild electric footshock stress was delivered during the dark portion of a 12:12 h light:dark cycle to C57BL/6 female mice that were infected with herpes simplex virus-type 1 (HSV). The studies were designed to correlate viral titer with both humoral and cell-mediated immune responses to HSV infection. Footshock was observed to result in decreased HSV-specific immunity. The numbers of leukocytes in spleens and draining popliteal lymph nodes of footshocked mice were depressed compared to both apparatus control and home cage control mice. A significant suppression of the HSV-specific cytotoxic T lymphocyte (CTL) response was observed in both the spleen and popliteal lymph nodes of footshocked mice. Serum IgM anti-HSV antibody titers were also depressed in footshocked mice. These changes were shown to be correlated with significantly increased viral titers in footshocked mice compared to control mice. These data demonstrate that administration of a relatively mild stressor is associated with depressed HSV-specific cellular and humoral immunity and is associated with increased pathogenicity.
Assuntos
Eletrochoque , Imunidade , Simplexvirus/imunologia , Animais , Anticorpos Antivirais/análise , Formação de Anticorpos , Feminino , Pé , Imunidade Celular , Contagem de Leucócitos , Camundongos , Camundongos Endogâmicos C57BL , Simplexvirus/patogenicidade , Simplexvirus/fisiologia , Baço/patologia , Linfócitos T Citotóxicos/patologia , Replicação ViralRESUMO
Changes in the cellular immune response associated with psychological stress were studied by using an academic stress model with medical students. The authors examined the expression of 2 proto-oncogenes, c-myc and c-myb, in peripheral blood leukocytes (PBLs) obtained from medical students at the time of examinations and at a baseline period approximately 1 month prior to the examinations. The level of messenger ribonucleic acid (mRNA) expression of both protooncogenes was significantly lower in PBLs obtained during examinations than in those from the baseline period. In addition, a significant decrease in the level of mRNA to the glucocorticoid receptor and gamma interferon was also found in the same preparations. The decrease in mRNA content of c-myc, c-myb, the glucocorticoid receptor, and gamma interferon in PBLs obtained from subjects during examinations is consistent with data from previous studies using the same model that have demonstrated a down-regulation of T-lymphocyte activation and proliferation in response to mitogens.
Assuntos
Ativação Linfocitária/genética , Proto-Oncogenes/genética , RNA Mensageiro/genética , Estresse Psicológico/complicações , Adulto , Feminino , Regulação da Expressão Gênica/fisiologia , Humanos , Ativação Linfocitária/imunologia , Masculino , Proto-Oncogene Mas , Proteínas Proto-Oncogênicas/genética , Proteínas Proto-Oncogênicas c-myb , Proteínas Proto-Oncogênicas c-myc/genética , Linfócitos T/imunologiaRESUMO
Numerous studies have sought to delineate the impact of neuroendocrine function on overall immune responsiveness. Using various murine models, we and others have previously shown that both adrenal-dependent and adrenal-independent mechanisms regulate components of the primary and memory cellular immune responses to herpes simplex virus type 1 (HSV-1) infection. We have extended these studies by determining the impact of 6-hydroxydopamine (6-OHDA)-induced peripheral sympathetic denervation on these responses. C57BL/6 mice treated with 6-OHDA (200 mg/kg) were inhibited in their ability to generate primary, HSV-specific cytotoxic T lymphocytes (CTL) in response to HSV infection. Sympathectomy also suppressed the activation and function of HSV-specific memory CTL (CTLm). In addition, administration of 6-OHDA resulted in a transient but substantial increase in levels of circulating corticosterone and hypothalamic Fos expression. Together, these findings suggest that peripheral sympathetic denervation may modulate immune function via activation of the hypothalamic-pituitary-adrenal (HPA) axis.
Assuntos
Herpes Simples/imunologia , Simplexvirus/imunologia , Linfócitos T Citotóxicos/imunologia , Animais , Herpes Simples/fisiopatologia , Masculino , Camundongos , Camundongos Endogâmicos C57BL , Neuroimunomodulação , Simpatectomia QuímicaRESUMO
This study investigated the memory T-cell proliferative response to several early and late Epstein-Barr virus (EBV) polypeptides. Blood samples were collected twice, 1 month before a 3-day block of examinations and again on the last day of the exam series. Ss were 25 healthy, EBV seropositive medical students. The proliferative response to 5 of the 6 EBV polypeptides significantly decreased during examinations. In addition, Ss high (above the median) in seeking support, as measured by the COPE, had lower proliferative responses to 3 EBV polypeptides (p17, p52/50, and p85), as well as higher levels of antibody to EBV virus capsid antigen. The data provide further evidence that psychological stress can modulate the cellular immune response to latent EBV.
Assuntos
Herpesvirus Humano 4/imunologia , Memória Imunológica/imunologia , Mononucleose Infecciosa/imunologia , Estresse Psicológico/complicações , Linfócitos T/imunologia , Adulto , Especificidade de Anticorpos/imunologia , Feminino , Comportamentos Relacionados com a Saúde , Humanos , Tolerância Imunológica/imunologia , Mononucleose Infecciosa/psicologia , Relações Interpessoais , Solidão , Masculino , Psiconeuroimunologia , Apoio Social , Estresse Psicológico/imunologiaRESUMO
The role of endogenous opioids in immunological mechanisms was examined by subjecting athymic (nu/nu) mice to chronic injections of the opioid agonist [Met5]-enkephalin (MET) or continuous opioid receptor blockade with naltrexone (NTX). After 8 days of treatment, neither excess peptide nor deprivation of opioids from receptors had any effect on body weight, spleen index (spleen to body weight ratio), total and differential white blood cell counts, and natural killer (NK) cell activity in peripheral blood or splenic lymphocytes. At 28 days, chronic treatment with MET or NTX had no effect on any of these parameters with the exception of an elevation from controls in NK cell activity in peripheral blood in mice receiving NTX, and subnormal NK cell activity related to splenic lymphocytes in the MET group. These results suggest that chronic exposure to an opioid agonist, or persistent opioid receptor blockade, have little influence on a variety of immunological properties in athymic mice, suggesting that native opioids such as MET do not play a marked role in defense mechanisms in the athymic mouse.
Assuntos
Contagem de Células Sanguíneas/efeitos dos fármacos , Encefalina Metionina/farmacologia , Células Matadoras Naturais/efeitos dos fármacos , Animais , Peso Corporal/efeitos dos fármacos , Contagem de Leucócitos/efeitos dos fármacos , Masculino , Camundongos , Camundongos Nus , Naltrexona/farmacologia , Antagonistas de Entorpecentes/farmacologia , Tamanho do Órgão/efeitos dos fármacos , Baço/citologia , Baço/efeitos dos fármacosAssuntos
Sistema Imunitário/fisiologia , Estresse Fisiológico/imunologia , Animais , Sobrevivência Celular , AMP Cíclico/análise , Herpesviridae/fisiologia , Herpesvirus Humano 4/imunologia , Humanos , Interferon gama/biossíntese , Células Matadoras Naturais/fisiologia , Fatores Inibidores da Migração de Leucócitos/biossíntese , Ativação Linfocitária , Neuropeptídeos/fisiologiaRESUMO
We have previously shown that restraint stress suppresses the activation of a polyclonal population of herpes simplex virus (HSV)-specific memory cytotoxic T lymphocytes (CTLm) to the lytic phenotype. We have extended these findings by demonstrating that this suppression occurs in two distinct HSV-specific CTLm populations that are generated in C57BL/6 mice in response to HSV infection and that recognize distinct epitopes expressed early in the HSV infection cycle. Moreover, these CTLm exhibited different levels of susceptibility to stress-induced suppression of activation. To elucidate the mechanisms responsible for this suppression, we have examined the effect of restraint on immunological components that are necessary for CTLm activation. We demonstrated that the expression of the T cell receptor (TCR), IL-2 receptor (IL-2R), and other accessory molecules involved in T cell activation were similar on CD8(+) T cell populations from both control and restrained groups of mice. However, splenic lymphoid cells from restrained mice generated significantly lower levels of IL-2, IL-4, IL-6, and gamma interferon (IFN-gamma) than did those cells from control, nonrestrained mice. The reduced ability to activate HSV-specific CTLm from mice subjected to restraint could be overcome by increasing the cell density and, thus, the lymphokine concentrations in these cultures. Overall, these findings suggest that restraint stress does not affect the inherent ability of an HSV-specific CTLm to be activated to the lytic phenotype; rather, the availability of lymphokines necessary to drive the activation process may be the limiting factor as to whether or not CTLm activation occurs. This stress-induced suppression of lymphokine production may not only play a role in inhibiting HSV-specific CTL activation but may also contribute to a diminution in the responsiveness and function of other components of immunological memory that are dependent on the presence of lymphokines.
Assuntos
Tolerância Imunológica/fisiologia , Memória Imunológica/fisiologia , Simplexvirus/imunologia , Estresse Psicológico/imunologia , Linfócitos T Citotóxicos/imunologia , Animais , Antígenos Virais/imunologia , Citotoxicidade Imunológica , Epitopos/imunologia , Ativação Linfocitária , Linfocinas/metabolismo , Masculino , Camundongos , Camundongos Endogâmicos C57BL , Psiconeuroimunologia , Restrição Física/efeitos adversos , Baço/imunologia , Linfócitos T Citotóxicos/metabolismoRESUMO
The herpes simplex virus (HSV)-specific cytolytic T lymphocyte (CTL) response in C57BL/6 (B6, H-2b) mice is restricted exclusively to the class I major histocompatibility complex (MHC) glycoprotein H-2Kb, with no detectable response restricted by H-2Db. However, analysis of the memory CTL population derived from B10.A(2R) (Kk Db) mice indicated that Db was a functional restriction element, and that failure to detect this subpopulation in B6 mice was not caused by the inability of HSV-derived antigens to associate with this self protein. Two long-term polyclonal CTL lines, one generated from B6 mice restricted by Kb and a second generated from 2R mice restricted by Db, were greater than 99% CD8+ and exhibited no natural killer (NK) cell activity. The adoptive transfer of either CTL line to naive recipients prior to infection in the hind footpads with HSV resulted in reduced levels of virus recovered from footpad tissue during the acute phase of infection and a reduction in latent HSV able to be reactivated from the sensory dorsal root ganglia (DRG) during the latent phase of infection. These results demonstrated not only that HSV antigen(s) may associate with Db, allowing restricted recognition controlled by this H-2 gene product, but also that functional Db-restricted CTL have the potential to exert biological activity in an environment in which they are not normally generated.
Assuntos
Alelos , Antígenos H-2/genética , Simplexvirus/imunologia , Linfócitos T Citotóxicos/imunologia , Animais , Linhagem Celular , Camundongos , Camundongos Endogâmicos C57BLRESUMO
The ability of highly lytic herpes simplex virus (HSV) cytolytic T lymphocytes to modulate the interaction between the murine host (adult C57BL/6 [H-2b] mice) and HSV type 1 Patton resulting in acute infection in the footpad and latent infection in the sensory lumbosacral dorsal root ganglia (L6, L5, L4, and L3) innervating the footpad was investigated. Results indicated that a critical threshold level of infectious HSV was required to establish infection. The adoptive transfer of cytolytic T lymphocytes derived from in vitro cultures after restimulation with HSV-infected, syngeneic stimulator cells exhibiting class I H-2-restricted, L3T4- Lyt-2+ HSV-specific cytolytic activity immediately before infection with a high dose of HSV reduced the levels of infectious HSV recovered from the footpad tissue during acute infection and the levels of latent HSV reactivated from the dorsal root ganglia to levels expected from mice infected with a low dose. Depletion of Lyt-2+ cells from the transferred population abrogated the protective ability, while depletion of L3T4+ cells had little effect. These results suggest that functionally lytic HSV-specific cytolytic T lymphocytes present at the time of HSV infection have the potential to participate in the control of the acute infection and in the subsequent establishment of latent infection.
Assuntos
Herpes Simples/imunologia , Linfócitos T Citotóxicos/imunologia , Animais , Pé/microbiologia , Gânglios Espinais/microbiologia , Imunidade Celular , Imunização Passiva , Camundongos , Simplexvirus/crescimento & desenvolvimento , Simplexvirus/imunologia , Linfócitos T Citotóxicos/classificaçãoRESUMO
The simian virus 40 (SV40) large T antigen was used as an immunogenic vector to express a herpes simplex virus type 1 (HSV-1) glycoprotein B (gB), H-2Kb-restricted cytotoxic T lymphocyte (CTL) recognition epitope corresponding to amino acid residues 498-505. Immunization of naive, C57BL/6 mice with a cell line, B6/350gB, expressing the chimeric T antigen was able to induce the generation of gB498-505-specific CTL in both the lymph nodes and the spleen. Splenic-derived, gB498-505-specific memory CTL (CTLm) were detected in these mice for at least 6 months following immunization at a slightly lower frequency than in those mice immunized with infectious HSV-1. B6/350gB was also able to activate in vitro gB498-505-specific memory CTL obtained from mice previously challenged with HSV. Overall, these findings support the use of a chimeric T antigen as a vector in determining the immunogenic potential of individual CTL epitopes and to assess their potential contribution in inducing a protective immune response in vivo.
Assuntos
Antígenos Virais/imunologia , Herpesvirus Humano 1/imunologia , Memória Imunológica/imunologia , Vírus 40 dos Símios/imunologia , Linfócitos T Citotóxicos/imunologia , Sequência de Aminoácidos , Animais , Antígenos Virais de Tumores/imunologia , Linhagem Celular , Epitopos , Linfonodos/citologia , Linfonodos/imunologia , Camundongos , Camundongos Endogâmicos C57BL , Dados de Sequência Molecular , Baço/citologia , Baço/imunologia , Proteínas do Envelope Viral/imunologiaRESUMO
A panel of herpes simplex virus type 1 (HSV-1)-specific, CD8+, major histocompatibility complex class I (H-2Kb)-restricted cytotoxic T-lymphocyte (CTL) clones was derived from HSV-1-immunized C57BL/6 (H-2b) mice in order to identify the HSV-1 CTL recognition epitope(s) which confers type specificity. HSV-1 x HSV-2 intertypic recombinants were used to narrow the region encoding potential CTL recognition epitopes to within 0.51 to 0.58 map units of the HSV-1 genome. Using an inhibitor of viral DNA synthesis and an ICP6 deletion mutant, the large subunit of ribonucleotide reductase (ICP6, RR1) was identified as a target protein for these type-specific CTL. Potential CTL recognition epitopes within RR1 were located on the basis of the peptide motif predicted to bind to the MHC class I H-2Kb molecule. A peptide corresponding to residues 822 to 829 of RR1 was shown to confer susceptibility on H-2Kb-expressing target cells to lysis by the type 1-specific CTL. On the basis of a comparison of the HSV-1 RR1 epitope (residues 822 to 829) with the homologous sequence of HSV-2 RR1 (residues 828 to 836) and by the use of amino acid substitutions within synthetic peptides, we identified HSV-1 residue 828 as being largely responsible for the type specificity exhibited by HSV-1-specific CTL. This HSV-1 RR1 epitope, when expressed in recombinant simian virus 40 large T antigen in primary C57BL/6 cells, was recognized by the HSV-1 RR1-specific CTL clones. These results indicate that an early HSV protein with enzymatic activity provides a target for HSV-specific CTL and that type specificity is dictated largely by a single amino acid.
Assuntos
Epitopos , Herpesvirus Humano 1/imunologia , Ribonucleotídeo Redutases/imunologia , Linfócitos T Citotóxicos/imunologia , Proteínas Virais/imunologia , Sequência de Aminoácidos , Animais , Antígenos Transformantes de Poliomavirus/imunologia , Dactinomicina/farmacologia , Epitopos/genética , Antígenos H-2/imunologia , Herpesvirus Humano 1/genética , Camundongos , Camundongos Endogâmicos C57BL , Dados de Sequência Molecular , Polimorfismo GenéticoRESUMO
Numerous studies have sought to delineate the impact of neuroendocrine function on overall immune responsiveness. Using various murine models, we and others have previously shown that both adrenal-dependent and adrenal-independent mechanisms associated with psychological stress modulate components of both the primary and memory cellular immune responses to herpes simplex virus type 1 (HSV-1) infection. We have extended these studies by determining the impact of 6-hydroxydopamine (6-OHDA)-mediated peripheral sympathetic denervation on both responses. C57BL/6 mice treated with 6-OHDA (200 mg/kg) exhibited reduced generation of both primary lymph node- and splenic-derived cytotoxic T lymphocytes (CTL) following a local (footpad) and systemic HSV infection, respectively. 6-OHDA also suppressed activation of HSV-specific memory CTL (CTLm). In both models, alterations in cytokine production and lymphocyte subset distribution were also observed. Administration of 6-OHDA also resulted in substantial but transient activation of the hypothalamic-pituitary-adrenal (HPA) axis as was indicated by a dramatic elevation of serum corticosterone and hypothalamic Fos expression. Moreover, the corticosterone levels were directly correlated with the extent of CTLm activation. Together, these findings suggest that peripheral sympathetic denervation alters immune function through activation of the HPA axis.
Assuntos
Herpes Simples/imunologia , Memória Imunológica/imunologia , Sistema Nervoso Simpático/imunologia , Linfócitos T Citotóxicos/imunologia , Animais , Células Cultivadas , Corticosterona/sangue , Ensaio de Imunoadsorção Enzimática , Herpes Simples/sangue , Interferon gama/análise , Interferon gama/biossíntese , Interleucina-2/análise , Interleucina-2/biossíntese , Interleucina-4/análise , Interleucina-4/biossíntese , Interleucina-6/análise , Interleucina-6/biossíntese , Linfócitos/metabolismo , Masculino , Camundongos , Camundongos Endogâmicos C57BL , Oxidopamina , Simpatectomia Química , Linfócitos T Citotóxicos/virologiaRESUMO
Using a murine model, we have previously shown that restraint stress is able to suppress the development of herpes simplex virus (HSV)-specific cytotoxic T lymphocytes (CTL) and natural killer (NK) cell activity in the popliteal lymph nodes following local footpad infection. These studies of the primary cell-mediated immune response to HSV infection have been extended to examine the effects of a similar stressor on the development of HSV-specific memory CTL (CTLm) following local and systemic HSV infection. In addition, the effect of stress on HSV-specific CTLm localization and proliferation in the popliteal lymph node following reexposure to HSV was investigated. Lastly, the ability to stimulate HSV-specific CTLm to the lytic phenotype under conditions of restraint stress was examined. Restraint stress did not inhibit the generation of HSV-specific CTLm. However, restraint stress inhibited the ability to activate CTLm to the lytic phenotype. In HSV seropositive mice (primed prior to stress), restraint stress prevented the in vivo activation and/or migration of HSV-specific CTLm in the popliteal lymph nodes. These findings demonstrate that activation of HSV-specific immunological memory can be inhibited by physiological changes associated with stress. Such immune inhibition may provide a possible mechanism for the development of recrudescent herpetic disease.