Proteome-wide analysis of the serological response to vaccinia and smallpox

被引:128
作者
Huw Davies, D.
Molina, Douglas M.
Wrammert, Jens
Miller, Joe
Hirst, Siddiqua
Mu, Yunxiang
Pablo, Jozelyn
Unal, Berkay
Nakajima-Sasaki, Rie
Liang, Xiaowu
Crotty, Shane
Karem, Kevin L.
Damon, Inger K.
Ahmed, Rafi
Villarreal, Luis
Felgner, Philip L.
机构
[1] Univ Calif Irvine, Dept Med, Div Infect Dis, Ctr Virus Res, Irvine, CA 92697 USA
[2] ImmPORT Therapeut, Irvine, CA USA
[3] Emory Univ, Sch Med, Emory Vaccine Ctr, Atlanta, GA 30322 USA
[4] Emory Univ, Sch Med, Dept Microbiol & Immunol, Atlanta, GA 30322 USA
[5] La Jolla Inst Allergy & Immunol, San Diego, CA USA
[6] CDC, Poxvirus Program, Atlanta, GA 30333 USA
关键词
antibody; antigen; poxviruses; protein microarray; vaccine;
D O I
10.1002/pmic.200600926
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
The eradication of smallpox by vaccination with vaccinia virus was probably one of the greatest achievements of vaccinology. However, the immunological basis of this protection is not fully understood. To this end, we have used protein microarrays of the vaccinia (Western Reserve, WR) proteome to profile antibody reactivities after primary infection or boosting with the licensed smallpox vaccine, Dryvax (R), and with archival convalescent smallpox sera. Some 25 antigens were consistently recognized by Dryvax (R) sera, of which half were envelope proteins (notably, H3, A13, B5, and D8). The remainder consisted mainly of core proteins (e.g. A10, L4, and I1), proteins involved in intracellular morphogenesis (A11, D13), and the A-type inclusion protein, WR148. Convalescent smallpox sera also detected vaccinia antigens on the array, consistent with the notion that there is serological cross-reactivity between these two orthopox species that underlies protection. Moreover, the profiles of immunodominant antigens recognized by variola-infected individuals and Dryvax (R) vaccinees were indistinguishable. This is the first description of antibody-specificity profiles induced after smallpox infection. The array data indicate that a significant component of the antibody response is not involved in virus neutralization, although these antigens should be considered alongside the envelope proteins as potential candidates for diagnostic and vaccine applications.
引用
收藏
页码:1678 / 1686
页数:9
相关论文
共 32 条
[1]   Shared modes of protection against poxvirus infection by attenuated and conventional smallpox vaccine viruses [J].
Belyakov, IM ;
Earl, P ;
Dzutsev, A ;
Kuznetsov, VA ;
Lemon, M ;
Wyatt, LS ;
Snyder, JT ;
Ahlers, JD ;
Franchini, G ;
Moss, B ;
Berzofsky, JA .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2003, 100 (16) :9458-9463
[2]   Obligatory requirement for antibody in recovery from a primary poxvirus infection [J].
Chaudhri, Geeta ;
Panchanathan, Vijay ;
Bluethmann, Horst ;
Karupiah, Gunasegaran .
JOURNAL OF VIROLOGY, 2006, 80 (13) :6339-6344
[3]   Vaccinia virus proteome: Identification of proteins in vaccinia virus intracellular mature virion particles [J].
Chung, CS ;
Chen, CH ;
Ho, MY ;
Huang, CY ;
Liao, CL ;
Chang, W .
JOURNAL OF VIROLOGY, 2006, 80 (05) :2127-2140
[4]   The nonreplicating smallpox candidate vaccines defective vaccinia Lister (dVV-L) and modified vaccinia Ankara (MVA) elicit robust long-term protection [J].
Coulibaly, S ;
Brühl, P ;
Mayrhofer, J ;
Schmid, K ;
Gerencer, M ;
Falkner, FG .
VIROLOGY, 2005, 341 (01) :91-101
[5]   Cutting edge: Long-term B cell memory in humans after smallpox vaccination [J].
Crotty, S ;
Felgner, P ;
Davies, H ;
Glidewell, J ;
Villarreal, L ;
Ahmed, R .
JOURNAL OF IMMUNOLOGY, 2003, 171 (10) :4969-4973
[6]   Vaccinia virus H3L envelope protein is a major target of neutralizing antibodies in humans and elicits protection against lethal challenge in mice [J].
Davies, DH ;
McCausland, MM ;
Valdez, C ;
Huynh, D ;
Hernandez, JE ;
Mu, YX ;
Hirst, S ;
Villarreal, L ;
Felgner, PL ;
Crotty, S .
JOURNAL OF VIROLOGY, 2005, 79 (18) :11724-11733
[7]   Profiling the humoral immune response to infection by using proteome microarrays: High-throughput vaccine and diagnostic antigen discovery [J].
Davies, DH ;
Liang, XW ;
Hernandez, JE ;
Randall, A ;
Hirst, S ;
Mu, YX ;
Romero, KM ;
Nguyen, TT ;
Kalantari-Dehaghi, M ;
Crotty, S ;
Baldi, P ;
Villarreal, LP ;
Felgner, PL .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2005, 102 (03) :547-552
[8]   Immunogenicity of a highly attenuated MVA smallpox vaccine and protection against monkeypox [J].
Earl, PL ;
Americo, JL ;
Wyatt, LS ;
Eller, LA ;
Whitbeck, JC ;
Cohen, GH ;
Eisenberg, RJ ;
Hartmann, CJ ;
Jackson, DL ;
Kulesh, DA ;
Martinez, MJ ;
Miller, DM ;
Mucker, EM ;
Shamblin, JD ;
Zwiers, SH ;
Huggins, JW ;
Jahrling, PB ;
Moss, B .
NATURE, 2004, 428 (6979) :182-185
[9]   Smallpox vaccine-induced antibodies are necessary and sufficient for protection against monkeypox virus [J].
Edghill-Smith, Y ;
Golding, H ;
Manischewitz, J ;
King, LR ;
Scott, D ;
Bray, M ;
Nalca, A ;
Hooper, JW ;
Whitehouse, CA ;
Schmitz, JE ;
Reimann, KA ;
Franchini, G .
NATURE MEDICINE, 2005, 11 (07) :740-747
[10]   Highly attenuated smallpox vaccine protects rabbits and mice against pathogenic orthopoxvirus challenge [J].
Empig, C ;
Kenner, JR ;
Perret-Gentil, M ;
Youree, BE ;
Bell, E ;
Chen, A ;
Gurwith, M ;
Higgins, K ;
Lock, M ;
Rice, AD ;
Schriewer, J ;
Sinangil, F ;
White, E ;
Buller, RM ;
Dermody, TS ;
Isaacs, SN ;
Moyer, RW .
VACCINE, 2006, 24 (17) :3686-3694