Displaying publications 1 - 20 of 1201 in total

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  1. POND WL, RUSS SB, LANCASTER WE, AUDY JR, SMADEL JE
    Am J Hyg, 1954 Jan;59(1):17-25.
    PMID: 13124320
    Matched MeSH terms: Antibodies*; Antibodies, Neutralizing*
  2. HALE JH, WITHERINGTON DH
    Ann Trop Med Parasitol, 1954 Mar;48(1):15-20.
    PMID: 13149114
    Matched MeSH terms: Antibodies*
  3. Smithburn KC
    Am J Hyg, 1954 Mar;59(2):157-63.
    PMID: 13138582
    Matched MeSH terms: Antibodies*; Antibodies, Neutralizing*
  4. Gordon Smith CE, Turner LH, Armitage P
    Bull World Health Organ, 1962;27:717-27.
    PMID: 13993152
    Because of the risk of introduction of yellow fever to South-East Asia, comparative studies were made of yellow fever vaccination in Malayans who had a high prevalence of antibody to related viruses and in volunteers without related antibody. The proportions of positive neutralizing antibody responses to subcutaneous vaccination with 17D vaccine were not significantly different between volunteers with and without heterologous antibody but the degree of antibody response was greater in those without. The ID(50) of 17D in both groups was about 5 mouse intracerebral LD(50). Multiple puncture vaccination with 17D gave a much lower response rate than subcutaneous vaccination in volunteers with heterologous antibody. In both groups subcutaneous doses of about 50 mouse intracerebral LD(50) gave larger antibody responses than higher doses. The neutralizing indices and analysis of results were calculated by a method based on the survival time of the mice. This method, which has advantages over that of Reed & Muench, is fully described in an annex to this paper.
    Matched MeSH terms: Antibodies, Neutralizing*
  5. Gordon Smith CE, McMahon DA, Turner LH
    Bull World Health Organ, 1963;29:75-80.
    PMID: 14043754
    In view of the risk of introduction of yellow fever into South-East Asia, comparative studies have been made of yellow fever vaccination in Malayan volunteers with a high prevalence of antibody to related viruses and in volunteers without related antibody. In a previous paper the neutralizing antibody responses of these volunteers were reported. The present paper describes the haemagglutinin-inhibiting (HI) antibody responses of the same groups of volunteers and discusses the relationship of these responses to the neutralizing antibody responses.The HI responses to yellow fever following vaccination closely paralleled the neutralizing antibody responses whether vaccination was subcutaneous or by multiple puncture. Volunteers with a high level of YF HI antibody due to infection with other group B viruses were found to be less likely to show a significant YF HI response than those without antibody. 90% of HI responses could be detected by the 21st day after vaccination.As with neutralizing antibody responses, volunteers given vaccine doses of 50-500 mouse intracerebral LD(50) subcutaneously gave greater responses than those given higher doses.
    Matched MeSH terms: Antibodies*
  6. SINGH S, KHUAN OY
    Med J Malaysia, 1964 Jun;18:251-61.
    PMID: 14199443
    Matched MeSH terms: Antibodies*
  7. COLLINS WE, SKINNER JC, GUINN EG, DOBROVOLNY CG, JONES FE
    J Parasitol, 1965 Feb;51:81-4.
    PMID: 14259488
    Matched MeSH terms: Antibodies*
  8. Lim Teong Wah
    Med J Malaya, 1965 Mar;19(3):188-90.
    PMID: 4220471
    Matched MeSH terms: Antibodies*
  9. Pacheco G, Danaraj TJ
    Am J Trop Med Hyg, 1966 May;15(3):355-8.
    PMID: 5938434
    Saline extracts of ether-treated Dirofilaria immitis, Ascaris suum, and Ancylostoma spp. were used in indirect hemagglutination tests of serum from 164 patients with a diagnosis of eosinophilic lung and 114 persons with other diseases or no disease (blood donors). In the first group, positive reactions with one, two or all three antigens were obtained in 89 percent of cases and the titers, at medium or high levels in 77 percent, decreased after treatment with diethylcarbamazine. In the other group, antibodies were demonstrable in the serum of only 22 percent of cases and titers usually were low. These observations indicate the presence of several antigen-antibody systems, some of which appear to be specific. With extracts of Dirofilaria the indirect hemagglutination and the complement-fixation tests were similar in sensitivity and specificity, but the results from neither test appeared to indicate infection with a specific worm.
    Matched MeSH terms: Antibodies*
  10. Singh M, Zaman V, Goh TK, Kheng CS
    Med J Malaya, 1967 Dec;22(2):115-7.
    PMID: 4231976
    Matched MeSH terms: Antibodies/analysis*
  11. Guest MF, Cheong WH, Fredericks H, Chin LK, Sulzer AJ
    Med J Malaya, 1968 Mar;22(3):248-9.
    PMID: 4234386
    Matched MeSH terms: Antibodies
  12. Tan DS, Lim TW, Ahluwalia P, Lee GC
    Med J Malaya, 1968 Jun;23(4):269-75.
    PMID: 4235589
    Matched MeSH terms: Antibodies/analysis
  13. Okuno T, Okada T, Kondo A, Suzuki M, Kobayashi M, Oya A
    Bull World Health Organ, 1968;38(4):547-63.
    PMID: 5302450
    The immunological characteristics of 26 strains of Japanese encephalitis virus (JEV) isolated in Japan and Malaya between 1935 and 1966 have been investigated mainly by the antibody-absorption variant of the haemagglutination-inhibition test, and to a certain extent also by conventional haemagglutination-inhibition and complement-fixation tests. The antibody-absorption technique shows promise as a routine method for the immunotyping of JEV.At present, two immunotypes can be distinguished. One comprises 2 strains, Nakayama-NIH and I-58, and is designated as the I-58 immunotype. The other immunotype, JaGAr 01, comprises 17 strains which share the characteristics of the JaGAr 01 strain, including one subline of the Nakayama strain, Nakayama-Yakken. The Nakayama-RFVL strain was found to have the characteristics of both immunotypes. The I-58 immunotype differs more markedly from related arboviruses, such as the Murray Valley encephalitis virus and the West Nile Eg101 strain, than does the JaGAr 01 immunotype.Evidence is presented which suggests that a given JEV strain can change immunotype on repeated passage through mice.
    Matched MeSH terms: Antibodies
  14. Yamanouchi K, Fukuda A, Kobune F, Hikita M, Shishido A
    Jpn. J. Med. Sci. Biol., 1969 Apr;22(2):117-21.
    PMID: 4981321
    Matched MeSH terms: Antibodies/analysis*
  15. Strauss JM, Alexander AD, Rapmund G, Gan E, Dorsey AE
    Am J Trop Med Hyg, 1969 Sep;18(5):703-7.
    PMID: 5817889
    Matched MeSH terms: Antibodies/analysis*
  16. Tan DS
    Bull World Health Organ, 1969;40(6):899-902.
    PMID: 5307602
    Epidemiological studies of human leptospirosis have generally been limited to countries with specialized laboratories employing the microscopic-agglutination (MA) test. The sensitized-erythrocyte-lysis (SEL) test is much simpler for routine hospital laboratories to carry out and it has been found valuable in the diagnosis of human leptospirosis. This paper reports the results of studies of the SEL test as an epidemiological tool in serological surveys.The results showed that the significant SEL titre was 1:80 and that the sensitivity of the test depended possibly on the antigen preparation and the amount of complement used. Most of the SEL antibodies were found to persist at significant titres for about 1 year after active infection, but less than half persisted longer than that. The SEL test is therefore useful for detecting recent infections and for indicating that stability of leptospirosis in an area.The endemicity of leptospirosis in West Malaysia was confirmed by the SEL test, based on the employment of 1:80 as the significant titre.
    Matched MeSH terms: Antibodies/analysis*
  17. Wong MM, Guest MF
    Trans R Soc Trop Med Hyg, 1969;63(6):796-800.
    PMID: 5368008
    Matched MeSH terms: Antibodies/analysis*
  18. Ching CY, Casals J, Bowen ET, Simpson DI, Platt GS, Way HJ, et al.
    Ann Trop Med Parasitol, 1970 Sep;64(3):263-8.
    PMID: 5500097
    Matched MeSH terms: Antibodies
  19. Rao TR
    Bull World Health Organ, 1971;44(5):585-91.
    PMID: 4400821
    Serological surveys have been widely used in South-East Asia to determine the presence and activity of arboviruses. The haemagglutination-inhibition test has been most frequently employed but complement-fixation and neutralization tests have also been used in some investigations.Although virus isolations provide the most conclusive evidence, they can be carried out in a few specialized centres only, and serological surveys are very important for studying the distribution of arboviruses.The surveys have shown that group B arboviruses (principally all four types of dengue, Japanese encephalitis, and West Nile) are widely prevalent. Dengue and Japanese encephalitis viruses are more widespread than West Nile virus, which was not known previously to extend east of India although recent survyes have shown that its range extends to Burma. Japanese encephalitis is frequent in most of South-East Asia but in India is found mainly in eastern and south-eastern parts of the country. Kyasanur Forest disease (KFD) and Langat viruses are the only tick-borne group B arboviruses definitely known to occur in the region, the former in India, the latter in Malaysia. KFD virus has been isolated only from a small focus in Mysore, although human and animal sera containing neutralizing antibodies to this virus have been found sporadically in widely scattered areas. Among the group A arboviruses, chikungunya and Sindbis have been detected in serological surveys, but the former has not yet been found in Malaysia.
    Matched MeSH terms: Antibodies/analysis
  20. Tan DS, Lopes DA
    PMID: 5082848
    Matched MeSH terms: Antibodies/isolation & purification
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