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Conference Paper: Prevalence of cytotoxin-producing Helicobacter pylori (Hp) strains detected by the anti-CagA Assay (ACAA) among patients with peptic ulcer disease and controls
Title | Prevalence of cytotoxin-producing Helicobacter pylori (Hp) strains detected by the anti-CagA Assay (ACAA) among patients with peptic ulcer disease and controls |
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Authors | |
Issue Date | 1995 |
Publisher | WB Saunders Co. The Journal's web site is located at http://www.elsevier.com/locate/gastro |
Citation | Digestive Disease Week and the 95th Annual Meeting of the American Gastroenterological Association, San Diego, CA, 14–17 May 1995. In Gastroenterology, 1995, v. 108 n. 4 S1, p. A70 How to Cite? |
Abstract | Background ELISA detecting anti-CagA protein antibody was previously
shown to yield a sensitivity of 96.2% and a specificity of 96.6% for
confh'mation of cytotoxin-producing (CT +) Hp infection. The ACAA was
performed in this study to document the prevalence of CT+ Hp infection
among the Chinese ulcer patients and controls in Hong Kong.
Materials & methods A cohort of lip+ duodenal ulcer (DIY), gastric ulcer
(GU) or asymptomatic normals (N) were selected for this study. Sera from
patients with DU (155 males [m] & 42 females [fl, mean age 41.7 yrs),
GU (57 m & 9 f, mean age 52.7 yrs), or N (52 m & 48 f, mean age 34.9
yrs) were used for ACAA. CagA (recombinant fragment) protein (1.25
ug/ml in carbonate buffer [pH 9.6]) was coated onto ELISA wells
overnight at 4°C. The wells were then quenched by PBS (pH7.4)/Tween
20 (0.1%) with 1$ BSA for 1 hr at room temperature (RT). Diluted
serum (1 in 75) in duplicates were added for incubation for 2 hr at RT.
The wells were washed and further incubated in peroxidase-tagged goat
anti-buman IgG antibody (1 in 2000) for 90 minutes at RT. The bound 2nd
antibody was identified by p-Nitrophenylphosphate. Finally, the plates
were read at 405rim. 100 sera from the N and documented Hp- were used
to determine the cut off level (mean + 2SD). Repeat assays on 6 negative
and 6 positive controls were performed to test the reproducibility.
Results The percentage of ACAA+ in these subjects were:
DU (n=197) GU (n=66) N (n=100) p value
ACAA+ 84 77.3 29.0 *<0.01
(*DU vs N and GU vs N). The ACA.A was highly reproducible (92%).
Conclusions CT+/-/p is present in both DU and GU patients significantly
more frequent than the N controls. These results would support CT+ lip
strains to be more ulcerogenic and that the CT must have played one of
the major direct or indirect offensive roles in the gastroduodenal mucosae. |
Persistent Identifier | http://hdl.handle.net/10722/102214 |
ISSN | 2023 Impact Factor: 25.7 2023 SCImago Journal Rankings: 7.362 |
DC Field | Value | Language |
---|---|---|
dc.contributor.author | Ching, CK | en_HK |
dc.contributor.author | Wong, BCY | en_HK |
dc.contributor.author | Lam, SK | en_HK |
dc.contributor.author | Ong, LY | en_HK |
dc.contributor.author | Lai, KC | en_HK |
dc.contributor.author | Hu, WH | en_HK |
dc.contributor.author | Lai, CL | en_HK |
dc.contributor.author | Lau, G | en_HK |
dc.date.accessioned | 2010-09-25T20:21:37Z | - |
dc.date.available | 2010-09-25T20:21:37Z | - |
dc.date.issued | 1995 | en_HK |
dc.identifier.citation | Digestive Disease Week and the 95th Annual Meeting of the American Gastroenterological Association, San Diego, CA, 14–17 May 1995. In Gastroenterology, 1995, v. 108 n. 4 S1, p. A70 | en_HK |
dc.identifier.issn | 0016-5085 | en_HK |
dc.identifier.uri | http://hdl.handle.net/10722/102214 | - |
dc.description.abstract | Background ELISA detecting anti-CagA protein antibody was previously shown to yield a sensitivity of 96.2% and a specificity of 96.6% for confh'mation of cytotoxin-producing (CT +) Hp infection. The ACAA was performed in this study to document the prevalence of CT+ Hp infection among the Chinese ulcer patients and controls in Hong Kong. Materials & methods A cohort of lip+ duodenal ulcer (DIY), gastric ulcer (GU) or asymptomatic normals (N) were selected for this study. Sera from patients with DU (155 males [m] & 42 females [fl, mean age 41.7 yrs), GU (57 m & 9 f, mean age 52.7 yrs), or N (52 m & 48 f, mean age 34.9 yrs) were used for ACAA. CagA (recombinant fragment) protein (1.25 ug/ml in carbonate buffer [pH 9.6]) was coated onto ELISA wells overnight at 4°C. The wells were then quenched by PBS (pH7.4)/Tween 20 (0.1%) with 1$ BSA for 1 hr at room temperature (RT). Diluted serum (1 in 75) in duplicates were added for incubation for 2 hr at RT. The wells were washed and further incubated in peroxidase-tagged goat anti-buman IgG antibody (1 in 2000) for 90 minutes at RT. The bound 2nd antibody was identified by p-Nitrophenylphosphate. Finally, the plates were read at 405rim. 100 sera from the N and documented Hp- were used to determine the cut off level (mean + 2SD). Repeat assays on 6 negative and 6 positive controls were performed to test the reproducibility. Results The percentage of ACAA+ in these subjects were: DU (n=197) GU (n=66) N (n=100) p value ACAA+ 84 77.3 29.0 *<0.01 (*DU vs N and GU vs N). The ACA.A was highly reproducible (92%). Conclusions CT+/-/p is present in both DU and GU patients significantly more frequent than the N controls. These results would support CT+ lip strains to be more ulcerogenic and that the CT must have played one of the major direct or indirect offensive roles in the gastroduodenal mucosae. | - |
dc.language | eng | en_HK |
dc.publisher | WB Saunders Co. The Journal's web site is located at http://www.elsevier.com/locate/gastro | en_HK |
dc.relation.ispartof | Gastroenterology | en_HK |
dc.title | Prevalence of cytotoxin-producing Helicobacter pylori (Hp) strains detected by the anti-CagA Assay (ACAA) among patients with peptic ulcer disease and controls | en_HK |
dc.type | Conference_Paper | en_HK |
dc.identifier.openurl | http://library.hku.hk:4550/resserv?sid=HKU:IR&issn=0016-5085&volume=108&spage=A70&epage=&date=1995&atitle=Prevalence+of+cytotoxin-producing+Helicobacter+pylori+(Hp)+strains+detected+by+the+anti-CagA+Assay+(ACAA)+among+patients+with+peptic+ulcer+disease+and+controls | en_HK |
dc.identifier.email | Ching, CK: chi_kong_ching@hotmail.com | en_HK |
dc.identifier.email | Lam, SK: deanmed@hku.hk | en_HK |
dc.identifier.email | Lai, KC: kclai@HKUCC.hku.hk | en_HK |
dc.identifier.email | Lai, CL: hrmelcl@hku.hk | en_HK |
dc.identifier.authority | Lai, CL=rp00314 | en_HK |
dc.description.nature | link_to_subscribed_fulltext | - |
dc.identifier.doi | 10.1016/0016-5085(95)22945-0 | - |
dc.identifier.hkuros | 9660 | en_HK |
dc.identifier.volume | 108 | en_HK |
dc.identifier.spage | 70 | en_HK |
dc.identifier.issnl | 0016-5085 | - |