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S T Dull

Publications and source records attributed to S T Dull.

6 recordsLinked to original sources
PubMed1999

Pilot study of local autologous tumor infiltrating lymphocytes for the treatment of recurrent malignant gliomas.

A prospective pilot study was performed in order to assess the safety of treating recurrent malignant gliomas (MGs) with locally infused autologous tumor infiltrating lymphocytes (TILs) and recombinant interleukin-2 (rIL-2). Six patients were entered between June 27, 1994 and June 2, 1995 and followed until July 1, 1998. At surgery an Ommaya reservoir was placed for later infusion of TILs and rIL-2. Following surgery, autologous TILs were expanded in vitro in the presence of rIL-2 and infused on treatment days 1 and 14, with concurrent rIL-2 infusions performed three times each week for one month. Following completion of immunotherapy all patients were offered chemotherapy. Phenotypic analysis demonstrated TILs to be T-lymphocytes (87-99% CD3+). Of these, 4 of 6 cases (67%) phenotyped as cytotoxic/suppressor T-lymphocytes (CD8+) and 2 of 6 cases (33%) phenotyped as helper/inducer T-lymphocytes (CD4+). TILs demonstrated limited selective cytotoxicity, with dose dependent cytotoxicity against autologous tumor, allogenic tumor and long term MG cell lines. There were no significant (Grade 3 or 4) complications. One patient developed transient low grade fevers, and 2 developed asymptomatic hydrocephalus. All patients developed transient and asymptomatic cerebral swelling, noted on the immediate post-treatment imaging studies. At three and six month follow-up, 3 patients responded with partial response, 2 demonstrated stable disease and 1 patient progressed. At long term follow-up, 1 patient had a complete response (45 month follow-up), 2 had a partial response (48 and 47 month follow-up) and 3 patients expired as a result of progressive disease (at 12, 12 and 18 months following immunotherapy). A relationship between subsequent chemotherapy or extent of resection to outcome was not apparent but could not be excluded. This pilot study demonstrated that locally infused autologous TILs and rIL-2 could be delivered without serious toxicity. Further studies are indicated to determine the safety and long term efficacy of TIL immunotherapy.

Adult↗
PubMed1995

Eosinophilic granuloma of the adult spine: a case report and review of the literature.

A 35-year-old patient who had progressive neck and shoulder pain and was neurologically intact was shown to have a C3 vertebral body osteolytic lesion. Open biopsy demonstrated an eosinophilic granuloma. The lesion was treated with external beam radiotherapy (1,000 cGy total dose). This case represents the thirteenth adult spinal eosinophilic granuloma reported in the literature. Spinal eosinophilic granuloma occurs more commonly in children. The characteristics of the 13 adult spinal eosinophilic cases reported suggest differences between the adult and childhood forms. Though rare, eosinophilic granuloma of the adult spine should be considered in the differential diagnosis of spinal osteolytic lesions.

Adult↗
PubMed1995

Preoperative oblique axial computed tomographic imaging for C1-C2 transarticular screw fixation: technical note.

C1-C2 transarticular screw fixation is an increasingly popular surgical method of treating atlantoaxial instability. When properly performed, it can safely provide fusion rates near 100%. However, the technique of screw insertion into this region allows only a small margin for error. Preoperative radiological assessment is essential to analyze the morphology of the region, assess for vertebral bony and vascular anomalies, and define the tolerances for the transarticular screws along their planned trajectory. As an adjunct to the preoperative planning of C1-C2 transarticular screw fixation, a unique, easily obtainable method of computed tomographic imaging, using thin-section oblique axial computed tomographic images of the C1-C2 region, is described.

Bone Screws↗
PubMed1991

Severe head injury: effect upon cellular immune function.

Infection is a major cause of morbidity following severe head injury. Although investigations have demonstrated central nervous system modulation of immune function, the effects of severe head injury on immune activity have not been well documented. This study prospectively investigated cellular immune function in 20 patients with isolated severe head injury. In vivo cellular immune status was determined by responses to delayed-type hypersensitivity (DTH) skin tests. In vitro studies included the effect of the lymphocyte mitogen, phytohaemagglutinin (PHA), on peripheral blood lymphocyte (PBL) phenotype expression and PBL blastogenesis. DTH skin testing demonstrated anergy to all antigens used during the first two weeks following head injury. Analysis of PBLs incubated with PHA demonstrated a decrease in the percent of PBL blastogenesis (p = 0.002), the percentage of cells marking as T-cells (p = 0.018), helper T-cells (p less than 0.001) and those expressing interleukin-2 receptors (p less than 0.001). There was a significant increase in the percentage of cells that marked as monocytes (p = 0.030), whereas there was no significant change in the percentage of B-cells, suppressor/cytotoxic T-cells, natural killer cells or in cells expressing the HLA-DR antigen. The infection rate was 55% with most occurring within 5 days of injury. The results of this study suggest that isolated severe head injury causes suppression of cellular immunity. The decrease in PHA stimulated PBL blastogenesis, helper T-cell phenotypic and interleukin-2 receptor expression, suggests suppression in early helper T-cell activation may be responsible for the high incidence of infection following severe head injury. The possible significance of increased monocyte phenotypic expression is discussed.

Adolescent↗
PubMedDate not supplied

Amplitude and latency characteristics of spinal cord motor evoked potentials in the rat.

The motor evoked potential (MEP) has become a valuable component of neurophysiological monitoring. A better understanding of the characteristics of the normal MEP is needed before one can fully appreciate the effects of injury on the MEP. We describe characteristic patterns of spinal cord MEPs, recorded epidurally, in response to transcranial (dura-to-palate) brain stimulation in a rat model. Series of signal averaged MEP responses at a duration of 100 microseconds were recorded at T10/11, T12/13, and L1/2 in 8 normal rats. We used a much greater range of current intensities (0.5-65 mA) than has been studied previously. Also, we studied the gradual development of the MEP wave form using smaller increments of current strength than have been reported previously. We confirmed in rats our earlier report in cats that long latency peaks appear first at low intensities while short latency peaks appear with higher intensities (Konrad et al. 1988). We also report average peak latencies over the range of stimulus intensities used for each recording level in each rat. In some rats, conduction velocities of several MEP peaks were calculated, and they range from 35 to 42 m/sec. These velocities are consistent with values reported in the literature for extrapyramidal pathways. Our rat model provides a method of measuring spinal cord potentials at three levels with no trauma to the spinal cord. Therefore, it can be used to repeatedly test motor function in chronic studies of spinal cord injury.

Animals↗