ABSTRACT
Severe combined immunodeficiency (SCID) is a heterogeneous group of disorders characterized by defect of T- and B-cell immunity. In many cases of autosomal recessive SCID, thus far described, the molecular alteration involves genes encoding for molecules that participate in the signal transduction. We report on a patient affected by a combined immunodeficiency, characterized by severe T-cell functional impairment, in spite of a close to normal number of circulating mature type T and B cells. NK cells were absent. Associated with the immunodeficiency, this patient also showed short stature characterized by very low growth velocity, delayed bone age and absence of increase of the plasma levels of Insulin growth factor-I (IGF-I) after growth hormone (GH) in vivo stimulation indicating peripheral hyporesponsiveness to GH. Evaluation of the protein tyrosine phosphorylation events occurring following either T-cell receptor (TCR) or GH receptor (GHR) triggering revealed striking abnormalities. No molecular alteration of GHR gene was found, thus suggesting the presence of postreceptorial blockage. Mutational screening and expression analysis failed to reveal any molecular alteration of JAK2 and STAT 5 A/B genes thus ruling out the involvement of these genes in the pathogenesis of this form of SCID. Mutational analysis of IL2Rgamma chain gene revealed the presence of a L183S missense mutation, thus indicating an atypical and a more complex clinical presentation of this X-linked form of SCID. At our knowledge, this is the first report on the GH hyporesponsiveness in this disease.
Subject(s)
Human Growth Hormone , Milk Proteins , Proto-Oncogene Proteins , Severe Combined Immunodeficiency/diagnosis , Severe Combined Immunodeficiency/immunology , Antigens, Differentiation, T-Lymphocyte/analysis , Body Height , Cells, Cultured , DNA-Binding Proteins/biosynthesis , DNA-Binding Proteins/genetics , Follow-Up Studies , Genetic Linkage , Human Growth Hormone/pharmacology , Humans , Infant , Interleukin Receptor Common gamma Subunit , Janus Kinase 2 , Lymphocyte Activation , Male , Pedigree , Phenotype , Phosphorylation , Protein-Tyrosine Kinases/genetics , RNA, Messenger/biosynthesis , Receptors, Antigen, T-Cell/immunology , Receptors, Interleukin-7/genetics , Receptors, Somatotropin/analysis , Receptors, Somatotropin/metabolism , STAT5 Transcription Factor , Severe Combined Immunodeficiency/genetics , T-Lymphocytes/immunology , Trans-Activators/biosynthesis , Trans-Activators/genetics , X ChromosomeABSTRACT
The proliferative responses of T lymphocytes of a subset of patients with CVID are abnormally low. This may be due to abnormalities in extracellular interactions or signalling defects downstream from membrane-associated receptors. Demonstrating that the T cell receptor signalling was normal, we observed no abnormal pattern of activation-induced tyrosine phosphorylation in cells from CVID patients. Moreover, the addition of exogenous IL-2 increased the low proliferation to mitogens, thus indicating the integrity of the IL-2R signalling apparatus. Attractin is a rapidly expressed T cell activation antigen involved in forming an association between T cells and monocytes. Twenty-four to 48 h after activation by CD3 cross-linking, attractin expression was not up-regulated on the cells of CVID patients despite normal up-regulation of CD25 and CD26. On control cells, however, attractin expression was up-regulated together with CD25 and CD26. The addition of the purified 175-kD attractin was capable of restoring the proliferative response of peripheral blood mononuclear cells following CD3 X-L in the presence of suboptimal concentrations of rIL-2 (10 and 20 U/ml). The effect was dose-dependent with the maximal effect at a concentration of 500 ng/ml, and present at a concentration as low as 50 ng/ml. Due to the likely role of attractin in cell guidance and amplification of the immune response, our results indicate that the lack of up-regulation of the molecule in patients with CVID may in turn affect any further step of productive immune response. Our finding may also imply a potential therapeutic role for this novel molecule.
Subject(s)
Common Variable Immunodeficiency/metabolism , Glycoproteins/biosynthesis , Glycoproteins/deficiency , T-Lymphocyte Subsets/immunology , T-Lymphocyte Subsets/metabolism , Adolescent , Adult , Antigens, CD19/biosynthesis , Biomarkers , CD3 Complex/biosynthesis , CD4 Antigens/biosynthesis , CD8 Antigens/biosynthesis , Cell Membrane/immunology , Cell Membrane/metabolism , Child , Common Variable Immunodeficiency/immunology , Dipeptidyl Peptidase 4/biosynthesis , Female , Glycoproteins/physiology , Humans , Immunophenotyping , Interleukin-2/pharmacology , Lymphocyte Activation , Male , Receptors, Interleukin-2/biosynthesis , Signal Transduction/immunology , T-Lymphocyte Subsets/pathologyABSTRACT
Human Nude/SCID (severe combined immunodeficiency) is the first severe combined immunodeficiency caused by mutation of the winged-helix-nude (WHN) gene, which is expressed in the thymus but not in the hematopoietic lineage. The disease is characterized by a T-cell defect, congenital alopecia, and nail dystrophy. A Nude/SCID patient who underwent bone marrow transplantation from the human leukocyte antigen-identical heterozygote brother was studied to investigate, in this unique model, the role of the thymus in immunologic reconstitution. Despite an increase in CD3(+), CD4(+), and CD8(+) cells, CD4(+) CD45 RA naive lymphocytes were not regenerated. Conversely, naive CD8(+) cells were normal. After an initial recovery, lymphocyte proliferation to mitogens progressively declined compared with controls and genotypically identical donor cells grown in the WHN(+/-) environment. Analysis of the T-cell receptor (TCR) repertoire of CD4(+) cells revealed that only 3 of 18 Vbeta families had an altered CDR3 heterogeneity length profile. Conversely, CD8(+) lymphocytes showed an abnormal distribution in most Vbeta families. These data indicate that the thymus is differentially required in the reconstitution of CD4(+) and CD8(+) naive subsets and in the maintenance of their TCR repertoire complexity. Taken together, these findings suggest that bone marrow transplantation is ineffective in the long-term cure of this form of SCID.
Subject(s)
Alopecia/genetics , DNA-Binding Proteins/deficiency , Severe Combined Immunodeficiency/genetics , Transcription Factors/deficiency , Alopecia/congenital , Animals , Antibody Formation , Consanguinity , DNA-Binding Proteins/genetics , DNA-Binding Proteins/physiology , Disease Models, Animal , Female , Follow-Up Studies , Forkhead Transcription Factors , Gene Rearrangement, T-Lymphocyte , Humans , Immunophenotyping , Infant, Newborn , Lymphocyte Activation , Male , Mice , Mice, Nude , Mice, SCID , Organ Specificity , Phenotype , Severe Combined Immunodeficiency/classification , Severe Combined Immunodeficiency/pathology , Severe Combined Immunodeficiency/therapy , Species Specificity , T-Lymphocytes/immunology , T-Lymphocytes/transplantation , Thymus Gland/abnormalities , Transcription Factors/genetics , Transcription Factors/physiology , Transplantation, HomologousABSTRACT
Congenital insensitivity to pain with anhidrosis (CIPA), a rare autosomal recessive disorder, is characterized by insensitivity to pain, self-mutilating behaviour, anhidrosis and recurrent hyperpyrexia. It is a hereditary sensory and autonomic neuropathy, also classified as HSAN, due to a defect of the receptor for nerve growth factor. CIPA is the first human genetic disorder caused by a defect in the neurotrophin signal transduction system. This is the first clinical report of CIPA patients characterized on molecular grounds. The clinical phenotypes of our patients show that CIPA is characterized by a multisystem involvement besides the nervous system, including bone fracture with slow healing, immunologic abnormalities, such as low response to specific stimuli, chronic inflammatory state ending in systemic amyloidosis. The molecular characterization allows a better understanding of most of the clinical features.
Subject(s)
Hypohidrosis/genetics , Pain Insensitivity, Congenital/genetics , Receptor, trkA/genetics , Abnormalities, Multiple/diagnosis , Abnormalities, Multiple/genetics , Child , Chromosome Aberrations/genetics , Chromosome Disorders , Female , Fractures, Spontaneous/diagnosis , Fractures, Spontaneous/genetics , Genes, Recessive/genetics , Hip Dislocation/diagnosis , Hip Dislocation/genetics , Humans , Hypohidrosis/diagnosis , Intellectual Disability/diagnosis , Intellectual Disability/genetics , Pain Insensitivity, Congenital/diagnosis , PhenotypeABSTRACT
In this study we report on a patient affected by a brain migration disorder and a T-cell activation deficiency presumably inherited as an autosomal recessive trait. The immunological evaluation revealed that the mitogen stimulation failed to induce a proper up-regulation of membrane expression of T-cell activation markers, and cell proliferation. This functional impairment was associated with abnormalities of the signal transduction process that follows T-cell receptor stimulation. A constitutive hyperphosphorylation of the Fyn tyrosine kinase was documented. This is the first report on a T-cell signaling abnormality associated with a developmental brain disorder. Whether the alteration of Fyn, which plays a role in both neurological and immunological systems, is responsible for either disorder remains to be elucidated.
Subject(s)
Brain Diseases, Metabolic, Inborn/metabolism , CD3 Complex/genetics , Immunologic Deficiency Syndromes/genetics , Protein-Tyrosine Kinases/metabolism , Proto-Oncogene Proteins/metabolism , Receptors, Antigen, T-Cell/genetics , Signal Transduction/genetics , Brain Diseases, Metabolic, Inborn/diagnosis , Brain Diseases, Metabolic, Inborn/enzymology , Brain Diseases, Metabolic, Inborn/immunology , Cell Movement/genetics , Child, Preschool , Epilepsy/genetics , Humans , Male , Phosphorylation , Protein-Tyrosine Kinases/genetics , Proto-Oncogene Proteins/genetics , Proto-Oncogene Proteins c-fynSubject(s)
Alopecia/genetics , Immunologic Deficiency Syndromes/genetics , Alopecia/congenital , Animals , Child, Preschool , DNA-Binding Proteins/genetics , Female , Forkhead Transcription Factors , Hair Follicle/metabolism , Humans , Mice , Mice, Nude , Molecular Sequence Data , Mutation , Phenotype , Transcription Factors/geneticsABSTRACT
Children affected by Down's syndrome (DS) have an increased susceptibility to viral or bacterial infections and leukemia, associated with several abnormalities of the immune system. We investigated whether the T cell defect was qualitative in nature and associated with abnormalities of the early events occurring during cell activation. The proliferative response of lymphocytes from DS individuals after CD3 cross-linking was clearly depressed, as already reported. In contrast, phorbol ester and ionomycin were able to induce cell cycle progression in DS, suggesting a defect in the early stages of the signal transduction through a T cell receptor/CD3 (TCR/CD3) complex upstream of protein kinase C activation. The functional impairment in DS was not related either to a decrease of circulating mature-type CD3+ cells, which express high levels of surface of CD3 molecules, or to a decrease of the CD4+ subpopulation. The analysis of phosphotyrosine-containing proteins after the cross-linking of CD3 molecules in DS lymphocytes revealed a partial signaling, characterized by increased phosphorylation of proteins of 42-44 kD, comparable to that observed in control subjects, but not of proteins of 70 and 21 kD. Moreover, although the "anti-anergic" gamma element of IL-2, IL-4, IL-7, and IL-15 receptors was normally tyrosine-phosphorylated during cell activation, the CD3 zeta-associated protein kinase (ZAP-70) was not. Our results indicate that in DS there is a T cell activation defect, characterized by partial signal transduction through a TCR/CD3 complex, and associated with a selective failure of ZAP-70 tyrosine phosphorylation.
Subject(s)
CD3 Complex/immunology , Down Syndrome/immunology , Lymphocyte Activation , Protein-Tyrosine Kinases/metabolism , T-Lymphocytes/immunology , Adolescent , Child , Child, Preschool , Down Syndrome/enzymology , Female , Humans , Male , Phosphorylation , Protein-Tyrosine Kinases/immunology , Receptors, Antigen, T-Cell/immunology , Signal Transduction , ZAP-70 Protein-Tyrosine KinaseABSTRACT
Liver disease may be found in patients with primary immunodeficiency syndromes because of the high risk of infection with hepatotropic viruses related to the treatment with blood derivatives. The prevalence of liver disease in these patients and its etiology, however, is still not completely understood. We have evaluated the prevalence and the etiology of liver disease in children with different forms of primary immunodeficiencies. Thirty patients included in the study underwent molecular studies to detect common hepatotropic viruses, including hepatitis C and G viruses. Liver involvement was found in 11 of 30 (36.6%) patients. All patients with liver disease had deficiencies of specific immunity, with a prevalence in this subgroup of 47.8%. Liver disease was more severe in patients with T and B cell combined immune disorders than in those with a selective T cell immunodeficiency. Moreover, the severity of the disease correlated with an overall more rapid fatal outcome. A viral etiology was found in only six of these patients, whereas in the remaining five patients, no cause of liver injury was identified. In the virally infected patients, hepatitis C virus was the most common viral agent. In patients with immunodeficiencies, there is a high prevalence of liver disease not fully explained on the basis of the common viral infections.
Subject(s)
Hepatitis, Chronic/etiology , Immunologic Deficiency Syndromes/complications , Adolescent , Biopsy , Child , Child, Preschool , Diagnosis, Differential , Female , Flaviviridae , Hepatitis C, Chronic/diagnosis , Hepatitis C, Chronic/etiology , Hepatitis, Chronic/diagnosis , Hepatitis, Viral, Human/diagnosis , Hepatitis, Viral, Human/etiology , Humans , Immunologic Deficiency Syndromes/diagnosis , Infant , Liver/pathology , Liver Function Tests , Male , Severe Combined Immunodeficiency/complications , Severe Combined Immunodeficiency/diagnosisABSTRACT
Dipeptidyl peptidase IV (CD26/DPP-IV) is an ectoenzyme expressed on different cell types. Signaling properties and functional consequences of the CD26 triggering have been elucidated mostly on T cells, where the molecule delivers a costimulatory signal that potentiates T-cell activation through the T-cell receptor. We conducted studies in the human hepatocarcinoma-derived PLC/PRF/5 cell line to examine the signal transduction through CD26 and its functional properties in the absence of other T-cell-specific membrane molecules. Engagement of CD26 in PLC/PRF/5 cells through a specific antibody induces tyrosine phosphorylation of several proteins with maximal intensity 15 minutes after the stimulation. This effect was under the negative regulatory control of CD45 tyrosine phosphatase, in that the addition of orthovanadate clearly enhanced the phosphorylation events. Using in vitro kinase assays with CD26 immunoprecipitates, we observed that a protein or proteins with kinase activity are coprecipitated with the CD26 molecule. In addition, unlike Jurkat T cells, in which CD26 expression exerts a protective effect against apoptosis, in PLC/PRF/5 cells CD26 occupancy delivers a potent apoptotic signal. This effect was also observed in HepG2 cells, thus indicating that it represents a more general phenomenon occurring in different liver neoplastic cell lines.
Subject(s)
Apoptosis , Carcinoma, Hepatocellular/pathology , Dipeptidyl Peptidase 4/physiology , Liver Neoplasms/pathology , Protein-Tyrosine Kinases/physiology , Carcinoma, Hepatocellular/enzymology , Dipeptidyl Peptidase 4/analysis , Humans , Leukocyte Common Antigens/analysis , Leukocyte Common Antigens/physiology , Liver Neoplasms/enzymology , Phosphorylation , Tumor Cells, Cultured , Type C Phospholipases/physiology , Tyrosine/metabolismABSTRACT
Viral infections may induce an acquired form of immunodeficiency, generally lasting a few weeks. In the more severe form, such as HIV infection, the immunodeficiency is permanent. Programmed death of T cells represents one of the mechanisms by which HIV determines the T cell functional impairment, finally resulting in the destruction of T cells. In this study, we evaluated whether an altered regulation of apoptosis was also implicated in the anergy associated with the common measles or varicella-zoster virus (VZV) infections in infancy. A spontaneous apoptosis of peripheral blood mononuclear cells was observed in children who had suffered from these infections as long as 6 mo after the acute disease. Apoptosis was demonstrated through analysis of cellular DNA content, morphologic evidence of cell nuclei shrinkage, and by analysis of DNA degradation. Stimulation of T cells through anti-CD4 MAb increased the number of apoptotic cells with a maximal effect 72 h after the stimulation. Our results suggest that apoptosis may account for the anergy that follows acute viral infections in infancy.
Subject(s)
Chickenpox/blood , Herpesvirus 3, Human , Leukocytes, Mononuclear/pathology , Measles/blood , Apoptosis , Chickenpox/pathology , Child , Child, Preschool , Female , Humans , Infant , Male , Measles/pathologyABSTRACT
BACKGROUND: Chronic hepatitis B (CHB) virus infection is associated with functional abnormalities of cell-mediated immunity, defective interferons alpha and gamma synthesis, and interleukin-2 receptor expression. In this study, interleukin-2 (IL-2) production and the role of adherent cells was evaluated in 25 children chronically infected with hepatitis B virus. METHODS: IL-2 activity was measured by bioassay in supernatants of phytohemoagglutinin-stimulated peripheral blood mononuclear cells. In a few patients, IL-2 concentration was also immunochemically determined. Coculture experiments using a mixture of adherent cells and lymphocytes from healthy children and patients with CHB were also performed. RESULTS: Children with CHB showed lower IL-2 production than healthy controls. In patients, IL-2 activity was 34.7 +/- 22.5 U/ml as compared to 152.6 +/- 78.5 U/ml of controls. Immunochemical quantitation of IL-2 confirmed a lower IL-2 production in patients. No correlation was found between the functional T-cell defect and the severity of liver damage, degree of viral replication, and duration of the disease. In co-culture experiments, adherent cells from HBsAg-positive patients inhibited IL-2 production following mitogen stimulation of control non-adherent cells by 67%. The inhibitory effect, mediated by patients adherent cells, was abolished by blocking with indomethacin prostaglandins, that are potent local immunomodulators released by adherent cells. CONCLUSIONS: Our results further support the observation that in children with CHB virus infection adherent cells play an important role in the inappropriate regulation of immune response, an effect being likely mediated by prostaglandins.