198 research outputs found
The requirement for phospholipase A2 for activation of the assembled NADPH oxidase in human neutrophils
CT and MRI of Hepatic Abscess in Patients with Chronic Granulomatous Disease
We describe the spectrum of radiologic appearances of hepatic
abscesses in patients with chronic granulomatous disease (CGD), a hereditary
immunodeficiency presenting in childhood that occurs at a rate of 1 in
200,000-250,000 live births and predisposes patients to infection with
catalase-positive organisms. CONCLUSION: Hepatic abscesses in patients with CGD
show an atypical radiologic appearance compared with sporadic hepatic abscesses,
and they are characterized by homogeneous enhancement and multiseptal
enhancement. In the appropriate clinical setting, the appearance of an enhancing
mass should suggest the possibility of a CGD-related hepatic absces
Hepatic abnormalities in patients with chronic granulomatous disease
Chronic granulomatous disease (CGD) is a rare congenital disorder characterized
by repeated bacterial and fungal infections. Aside from a high incidence of liver
abscess, little is known about hepatic involvement in CGD. The aim of this study
was to describe the spectrum of liver abnormalities seen in CGD. The charts of
194 patients with CGD followed at the NIH were reviewed, with a focus on liver
abnormalities. Liver enzyme elevations occurred on at least one occasion in 73%
of patients during a mean of 8.9 years of follow-up. ALT elevations were
generally transient. Although transient alkaline phosphatase (ALP) elevations
were also common, persistent ALP elevations lasting up to 17.6 years were seen in
25% of patients. Liver abscess occurred in 35% of patients. Drug-induced
hepatotoxicity was documented in 15% of patients but likely occurred more
frequently. Hepatomegaly was found in 34% and splenomegaly in 56% of patients.
Liver histology showed granulomata in 75% and lobular hepatitis in 90% of
specimens. Venopathy of the portal vein was common (80%) and associated with
splenomegaly. Venopathy of the central vein was also common (63%) and was
associated with the number of abscess episodes. Nodular regenerative hyperplasia
(NRH) was seen in 9 patients, including 6 of 12 autopsy specimens. CONCLUSION:
Liver enzyme abnormalities occur frequently in patients with CGD. In addition to
liver abscesses and granulomata, drug hepatotoxicity is likely underappreciated.
Vascular lesions such as venopathy and--to a lesser extent--NRH are common. The
cause and clinical consequences of venopathy await prospective evaluation
Reactive oxygen species in phagocytic leukocytes
Phagocytic leukocytes consume oxygen and generate reactive oxygen species in response to appropriate stimuli. The phagocyte NADPH oxidase, a multiprotein complex, existing in the dissociated state in resting cells becomes assembled into the functional oxidase complex upon stimulation and then generates superoxide anions. Biochemical aspects of the NADPH oxidase are briefly discussed in this review; however, the major focus relates to the contributions of various modes of microscopy to our understanding of the NADPH oxidase and the cell biology of phagocytic leukocytes
Surface Mol (CD11b/CD18) glycoprotein is up-modulated by neutrophils recruited to sites of inflammation in vivo
Inasmuch as the recruitment of polymorphonuclear leukocytes (PMNs) to inflammatory foci in vivo involves adhesion-dependent events (e.g., margination, diapedesis, and directed migration), we sought to characterize the relationship between the local accumulation of PMNs in sterile peritonitis and their surface expression of the adhesion-promoting plasma membrane glycoprotein. Mol (CD11b/ CD18). In an immunofluorescence analysis of PMNs isolated from rats injected intraperitoneally with sterile 1% glycogen solution, we detected a significant enhancement of surface Mol expression by exudative peritoneal PMNs. In contrast, no significant rise in Mol expression was noted over time by circulating intravascular PMNs (isolated simultaneously). However, these intravascular PMNs had the capacity to increase their surface Mol density upon exposure to peritoneal fiuid supernatant at 37°C. These results demonstrate that PMNs at sites of inflammation in vivo do up-modulate their surface expression of the adhesion-promoting Mol glycoprotein during their recruitment from the circulating, intravascular leukocyte pool.Peer Reviewedhttp://deepblue.lib.umich.edu/bitstream/2027.42/44502/1/10753_2004_Article_BF00916757.pd
Inherited p40phox deficiency differs from classic chronic granulomatous disease
Biallelic loss-of-function (LOF) mutations of the NCF4 gene, encoding the p40phox subunit of the phagocyte NADPH oxidase, have been described in only 1 patient. We report on 24 p40phox-deficient patients from 12 additional families in 8 countries. These patients display 8 different in-frame or out-of-frame mutations of NCF4 that are homozygous in 11 of the families and compound heterozygous in another. When overexpressed in NB4 neutrophil-like cells and EBV-transformed B cells in vitro, the mutant alleles were found to be LOF, with the exception of the p.R58C and c.120_134del alleles, which were hypomorphic. Particle-induced NADPH oxidase activity was severely impaired in the patients' neutrophils, whereas PMA-induced dihydrorhodamine-1,2,3 (DHR) oxidation, which is widely used as a diagnostic test for chronic granulomatous disease (CGD), was normal or mildly impaired in the patients. Moreover, the NADPH oxidase activity of EBV-transformed B cells was also severely impaired, whereas that of mononuclear phagocytes was normal. Finally, the killing of Candida albicans and Aspergillus fumigatus hyphae by neutrophils was conserved in these patients, unlike in patients with CGD. The patients suffer from hyperinflammation and peripheral infections, but they do not have any of the invasive bacterial or fungal infections seen in CGD. Inherited p40phox deficiency underlies a distinctive condition, resembling a mild, atypical form of CGD.info:eu-repo/semantics/publishedVersio
Inherited p40^{phox} deficiency differs from classic chronic granulomatous disease
Biallelic loss-of-function (LOF) mutations of the NCF4 gene, encoding the p40^{phox} subunit of the phagocyte NADPH oxidase, have been described in only 1 patient. We report on 24 p40^{phox}-deficient patients from 12 additional families in 8 countries. These patients display 8 different in-frame or out-of-frame mutations of NCF4 that are homozygous in 11 of the families and compound heterozygous in another. When overexpressed in NB4 neutrophil-like cells and EBV-transformed B cells in vitro, the mutant alleles were found to be LOF, with the exception of the p.R58C and c.120_134del alleles, which were hypomorphic. Particle-induced NADPH oxidase activity was severely impaired in the patients’ neutrophils, whereas PMA-induced dihydrorhodamine-1,2,3 (DHR) oxidation, which is widely used as a diagnostic test for chronic granulomatous disease (CGD), was normal or mildly impaired in the patients. Moreover, the NADPH oxidase activity of EBV-transformed B cells was also severely impaired, whereas that of mononuclear phagocytes was normal. Finally, the killing of Candida albicans and Aspergillus fumigatus hyphae by neutrophils was conserved in these patients, unlike in patients with CGD. The patients suffer from hyperinflammation and peripheral infections, but they do not have any of the invasive bacterial or fungal infections seen in CGD. Inherited p40^{phox} deficiency underlies a distinctive condition, resembling a mild, atypical form of CGD
Properties of murine intracisternal a particles. Electron microscopic appearance after critical point drying and platinum shadowing.
Transfer of murine intracisternal a particle phenotype in chloramphenicol-resistant cytoplasts.
Use of chloramphenicol resistant cytoplasts to transfer mouse intracisternal a particle (iap) phenotype. Abstr.
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