Polyclonal lymphoma confined to renal allograft: case report.
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Adult↗
Biomedical subjects
L Lauriola
Publications and source records attributed to L Lauriola.
Protein absorption by tubular mesonephric and metanephric structures in the human embryo. An immunohistochemical study.
The presence of different serum proteins in the cells of the proximal tubule of both meso- and metanephric nephrons in human embryos (7th-12th week of intrauterine life) was investigated using immunohistochemistry. Endogenous lysozyme, alpha-1-antitrypsin and ferritin were detected in mesonephric proximal tubules and, starting from the 8th week, also in metanephric proximal tubules. Our observations provide information concerning the appearance and distribution of tubular protein reabsorption during the early stages of development.
Embryo, Mammalian↗
Glial-like cells in sympathetic neural crest derivatives during human embryogenesis. Detection by S-100 immunohistochemistry.
The present study investigates at the light and electron microscopic levels the possible presence and distribution during human development of glial-like satellite cells in sympathetic neural crest derivatives by S-100 immunohistochemistry. From the earliest stages investigated, immunostained cells were detected inside sympathetic migrating masses and at their periphery, where they constituted a continuous layer isolating sympathetic elements from mesenchymal cells. The detection and peculiar distribution of these glial-like cells in developing sympathetic tissue could open new perspectives in the study of events linked to the migration and differentiation of some neural crest derivatives.
Cell Differentiation↗
Immunohistochemical localization of S-100-containing cells in non-nervous structures of the human eye.
The present study reports on the immunohistochemical distribution of S-100 antigen in non-nervous cell types within the human eye at light microscopy. In the cornea the antigen was confined to endothelial cells covering its posterior surface; the lens exhibited immunoreactivity restricted to the epithelial cells located beneath the anterior capsule. In the iris and ciliary body, S-100 was detected in stromal cells and epithelial cells of the pigmented inner layer in the former and inner epithelial cells bounding the posterior chamber in the latter.
Ciliary Body↗
S-100 protein in the testis. An immunochemical and immunohistochemical study.
S-100, a protein originally believed to be unique to the nervous system, has recently been found in extraneural presence of S-100 in the testis, namely in Leydig cells and in lymphatic endothelial cells, using immunohistochemical and immunochemical methods. We show that the protein in the testis is immunologically identical to brain S-100. The S-100-labelled cells in the testis exhibit morphological similarities with other cell types in different tissues known to contain S-100.
Animals↗
Satellite cells in the normal human adrenal gland and in pheochromocytomas. An immunohistochemical study.
In light of the recent finding of the S-100 antigen in satellite cells of the rat adrenal medulla, we looked for S-100-labelled cells in both the normal human adrenal medulla and in pheochromocytomas. Immunostaining enabled us to detect S-100-labelled satellite cells by both light and electron microscopy in a significant number of pheochromocytomas and, as expected, in the normal human adrenal medulla.
Adrenal Gland Neoplasms↗
Immunohistochemical distribution of S-100 antigen in the urinary system of man and rat.
The immunohistochemical distribution of S-100, a protein originally isolated from the brain, has been investigated at the light and electron microscopic levels in rat and man urinary systems. In both species the antigen essentially exhibited the same location, restricted, with different degrees of staining, to certain cells in the kidney, i.e. collecting tubules, thin limbs of Henle's loop and renal papillae.
Animals↗
Ia- and IgG-Fc receptor-positive accessory cell sustains peripheral T lymphocyte but not thymocyte mitogenesis induced by OKT3 monoclonal antibody.
The proliferative responses of human peripheral blood mononuclear cells (PBL) and thymocytes to OKT3 monoclonal antibody have been investigated. The PBL response to OKT3 was maximal after 72 hr while that of thymocytes was inappreciable at all times measured. Unlike phytohemagglutinin, OKT3 was unable to elicit the mitogenesis of adherent cell-depleted T cells in spite of the presence of exogenously added Interleukin 1 and/or Interleukin 2. The addition of autologous or heterologous adherent cells restored the OKT3 mitogenic response of peripheral purified T cells but not of thymocyte cultures. The adherent cell population that was able to sustain the OKT3-elicited T-cell mitogenesis was constituted by Ia-, Fc receptor-positive cells. These data suggest that the adherent cell-T cell interaction is mediated via the Fc portion of the OKT3 molecule. Furthermore, unlike peripheral T cells, T3-positive thymocytes, which represent the more mature. PHA-responsive subset within the thymus, are unable to cooperate with accessory cells when pulsed with OKT3 monoclonal antibody.
Antibodies, Monoclonal↗
Detection by S-100 immunolabelling of interdigitating reticulum cells in human thymomas.
In the light of recent findings concerning the presence of S-100 antigen in interdigitating reticulum cells (IRC's) in the normal human thymus, we investigated the possible presence of these cells in human thymomas. By the unlabelled antibody PAP method, using an anti-S-100 antiserum, both by light and electron microscopy we were able to demonstrate immunolabelled IRC's in the majority of spindle cell and in some round-oval cell thymomas. Keeping in mind the possible role of IRC's in intrathymic T-cell differentiation, the present findings could be relevant in the better comprehension of this thymic neoplasm.
Histocytochemistry↗
Immunohistochemical detection of folliculo-stellate cells in human pituitary adenomas.
In the light of recent findings concerning the presence of S-100 antigen in folliculo-stellate cells of the rat adenohypophysis, we investigated the possible presence of S-100-labelled cells in both the normal human adenohypophysis and in pituitary adenomas. Immunostaining enabled us to detect, with both light and electron microscopy, the presence of S-100-labelled folliculo-stellate cells in a significant number of pituitary adenomas, mostly growth-hormone secreting, and, as expected, in the normal human adenohypophysis.
Adenoma↗
Detection of S-100 labelled cells in nasopharyngeal carcinoma.
S-100 antigen containing cells with dendritic features, recognisable by morphological and immunohistochemical criteria as belonging to the Langerhans' or interdigitating reticulum cell type, have been found in undifferentiated nasopharyngeal carcinoma. The presence of these cells, which have a special function of antigen presentation in immune responses, may be involved in a possible modulation of nasopharyngeal carcinoma associated Epstein-Barr virus infection and host-tumour interactions.
Carcinoma↗
Glucocorticoid inhibitory action on the response to PHA of residual circulatory lymphocytes in renal transplant patients following immunosuppressive therapy.
The inhibitory effect of glucocorticoids on the in vitro response to phytohaemagglutinin of the residual circulating T lymphocytes in renal transplant patients during maintenance immunosuppressive therapy with glucocorticosteroids and azathioprine has been investigated. As in normal subjects, the steroid-induced inhibition of transplanted patients' lymphocyte response was inversely correlated with the mitogen concentration used. On the other hand, the response of the various lymphocyte preparations from transplanted patients appeared less inhibited by steroids than the corresponding preparations from normal subjects. The addition to the culture of the adherent cell product interleukin 1 was effective in removing to a similar extent the steroid inhibitory effect on lymphocytes from normal and transplanted subjects. Thus, the lesser inhibitory effect of glucocorticoids on transplanted patient lymphocytes could be explained by the higher percentages of monocytes present in all peripheral blood mononuclear cell preparations. These results suggest that during immunosuppressive therapy with glucocorticoids and azathioprine the residual circulating lymphocytes have a responsiveness to in vitro dexamethasone suppression similar to that of normal peripheral blood lymphocytes.
Antibodies, Monoclonal↗
Glucocorticoid inhibitory action on OKT3-stimulated peripheral blood lymphocytes from renal transplant patients.
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Antibodies, Monoclonal↗
Congenital epulis: an ultrastructural and immunohistochemical study.
In the light of recent findings concerning the presence of S-100 antigen in granular cell myoblastoma (GCM), we investigated by immunoperoxidase the presence of this antigen in a case of congenital epulis (CE). The absence of S-100 in CE granular cells is suggestive for antigenic differences with GCM. Upon ultrastructural investigation, bundles of collagen fibers were observed in the cytoplasm of CE granular cells and cells displaying features of initial cytoplasmic vacuolar transformation were also detected. Interstitial cells containing angulated bodies, a common finding in GCM, were not found.
Collagen↗
Modulation of glucocorticoid inhibitory action on human lymphocyte mitogenesis: dependence on mitogen concentration and T-cell maturity.
The inhibitory effect of glucocorticoids on the mitogenesis of human T cells derived from thymus and peripheral blood compartments have been investigated. The capacity of dexamethasone (Dex) (10(-7) M) of inhibiting the peripheral blood lymphocyte (PBL) mitogenesis was inversely correlated with the phytohemagglutinin (PHA) concentration used. Conversely, Dex completely (greater than 90%) inhibited the thymocyte mitogenesis, irrespective of PHA concentrations. T cells purified from PBL (M phi less than or equal to 1%) behaved as thymocytes regarding the Dex inhibitory pattern. The addition of macrophages (M phi) or interleukin 1 (IL1) was effective in removing the Dex inhibitory effect on T cells purified from PBL, but not on thymocytes. The higher corticosensitivity of thymocyte mitogenesis in comparison to PBL mitogenesis cannot be explained by differences in the relative number of M phi, but seems an intrinsic property of these less mature T cells.
Cell Survival↗
S-100 antigen labels neoplastic cells in liposarcoma and cartilaginous tumours.
S-100 antigen, originally believed to be unique to the nervous system, has recently been found in cell types of non-neuroectodermal origin such as chondrocytes and adipocytes. These findings suggested the possibility of detecting the antigen in tumours derived from such cells. Using the PAP method and an anti-ox brain S-100, the antigen was found in the cells of human chondrosarcomas, chondroblastomas and liposarcomas. In contrast, fibrous histiocytomas and fibrosarcomas, tested to verify the cellular specificity of the S-100 immunoreaction, did not exhibit S-100-containing cell types. The present data indicate the usefulness of the S-100 antigen as a diagnostic and investigative tool in defined neoplasms of non-neuroectodermal origin, such as chondroid tumours and liposarcoma.
Biopsy↗
Dissociation between coupled lymphocyte phenotypic and functional properties in Sézary cells.
Neoplastic lymphocytes derived from three patients suffering from Sézary syndrome were studied by immunologic and functional analysis. Populations of neoplastic T cells (greater than 90% as judged by morphologic criteria) were isolated from involved lymph nodes. Sézary cells expressed T3 and T4 but not T8 membrane antigens displaying the same phenotypic pattern of normal helper/inducer T cells. On the contrary the mitogenic response of Sézary cells to phytohemagglutinin appears lower than that exhibited by peripheral T lymphocytes. The amounts of interleukin 2 produced by Sézary cells were examined in two out of three cases: in one case it appeared similar to that produced by peripheral blood lymphocytes while in the other it was about one-half lower. Furthermore the capacity of dexamethasone at 10(-7) M in inhibiting T-cell mitogenesis was comparatively analyzed in T lymphocytes from Sézary lymph nodes, reactive lymph nodes, normal peripheral blood, and normal thymus. It was clearly apparent that the mitogenesis of Sézary cells, unlike that of peripheral blood lymphocytes and that of lymphocytes from reactive lymph nodes, was strongly inhibited by dexamethasone (greater than 70%); such inhibition was very similar to that observed for normal thymocytes. Taken together these results suggest that despite the phenotypic pattern of mature helper/inducer T cells, Sézary lymphocytes are functionally a less mature T-cell type.
Antigens, Surface↗
A human thymoma with prothymocyte-like infiltration.
We have examined a human thymoma, round-oval epithelial-type cell with moderate lymphocytic infiltration, whose major lymphocytic component (67%), unlike the minor one (33%), did not form rosettes with sheep red blood cells (E rosettes). However, these cells were of T-cell nature as indicated by the positive staining for both acid phosphatase and beta-glucuronidase, two well-accepted cytochemical markers for T cells. The non-E-rosetting lymphocytes expressed T 10, but not T 3 and T 6 antigens. Moreover, they lacked both peanut agglutinin and Fc-IgG receptors. On the contrary, 71 and 19% of the E-rosetting cells were PNA- and Fc-IgM-receptor positive, respectively. Furthermore, the non-E-rosetting cells were phytohemagglutinin unresponsive. The non-E-rosetting lymphocytes were larger (greater than 7 micron) than the E-rosetting cells and showed a different nuclear chromatin pattern. These immunological, cytochemical, and morphological features strikingly resemble those exhibited by cells (prothymocytes) normally found only in fetal thymus. On the basis of these findings we hypothesize the existence in this thymoma of a prothymocyte-like infiltration.
Acid Phosphatase↗