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. 2009 Mar 25;83(11):5388–5400. doi: 10.1128/JVI.02598-08

TABLE 1.

Clinical and pathological outcome in MVA-SIV-vaccinated macaques following SIVsmE660 challenge

Group and macaque MHC-Ia Survival (wks) Pathology or clinical findingsc
Gag-Pol
    H421 B*29 212 Pneumocystis pneumonia, LD
    H423 70 Bacterial bronchopneumonia, LD
    H457 107 Amyloidosis, lymphoid and intestinal
    H462 118 Enterocolitis
    18685 B*29 39 Bacterial endocarditis with microabscesses
    18894 84 Enteritis, mild SIVE, interstitial nephritis, LD
Env
    H422 450+ Healthy
    H424 72 Protozoal enteritis, interstitial pneumonia, SIV
    H453 B*29 66 Pneumocystis pneumonia, LD
    H456 B*29 450+ Low CD4 cell count
    18679 70 Multicentric lymphoma (liver, kidneys, heart)
    18681 149 Endocarditis, enteritis with intestinal amyloidosis
Gag-Pol-Env
    H425 B*29 73 Enteritis (Strongyloides), lymphoma
    H427 120 Enteritis, LD
    H448 123 Enteritis
    H452b 225 Suppurative arthritis, all other tissues WNL
    18661 B*08 75 Pneumocystis enteritis with amyloid (LP)
    18673 A*01, B*29 365 Cryptosporidial cholecystitis, pancreatitis, intestinal amyloidosis, colitis
Control
    H386b A*01 16 Anesthetic death, not SIV related
    H387 32 Severe bilateral bacterial pyelonephritis, LD
    H426 23 SIVE and SIV pneumonia
    H428 150 Cholangiohepatitis and enteritis (Cryptosporidium)
    18654 B*08 58 Severe enteritis with edema, crypt abscesses
    18655 16 SIVE and SIV pneumonia
a

All animals were genotyped for three of the MHC-I alleles associated with control of viremia and slow disease progression in SIV-infected macaques, Mamu-A*01, -B*08, and -B*29, as described in Materials and Methods.

b

Premature death, not directly related to SIV infection.

c

SIVE, SIV encephalitis; LD, lymphoid depletion; NA, not applicable; WNL, within normal limit; LP, lamina propria.